ChemicalBook > CAS DataBase List > (1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine

(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine

Product Name
(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine
CAS No.
167316-27-0
Chemical Name
(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine
Synonyms
(S,S)-TSDPEN;N-((1S,2S)-2-amino-1,2-diphenylethyl)-4-methylbenzenesulfonamide;(1S,2S)-N-(p-Toluenesulfonyl)-1,2-diphenylethanediamine;(1S,2S)-TSDPEN;2S)-(+)-N-p-Tosyl-1;2-diphenylethylenediaMine;(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-;(1S,2S)-N-P-TOSYL-1,2-DIPHENYLETHYLENE-D;(1S,2S)-N-Tosyl-1,2-diphenylethylene-1,2-diamine;(1S,2S)-(-)-N-P-TOSYL-1,2-DIPHENYLETHYLENEDIAMINE
CBNumber
CB4775946
Molecular Formula
C21H22N2O2S
Formula Weight
366.48
MOL File
167316-27-0.mol
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(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine Property

Melting point:
128-131 °C (lit.)
alpha 
61.5 º (C=1, CH2Cl2)
Boiling point:
537.3±60.0 °C(Predicted)
Density 
1.1440 (rough estimate)
refractive index 
30 ° (C=1, CHCl3)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Solubility in hot Acetonitrile (almost transparency).
pka
10.76±0.50(Predicted)
form 
crystal
color 
white
optical activity
[α]20/D +35°, c = 1 in chloroform
InChI
InChI=1S/C21H22N2O2S/c1-16-12-14-19(15-13-16)26(24,25)23-21(18-10-6-3-7-11-18)20(22)17-8-4-2-5-9-17/h2-15,20-21,23H,22H2,1H3/t20-,21-/m0/s1
InChIKey
UOPFIWYXBIHPIP-SFTDATJTSA-N
SMILES
C1(S(N[C@@H](C2=CC=CC=C2)[C@@H](N)C2=CC=CC=C2)(=O)=O)=CC=C(C)C=C1
CAS DataBase Reference
167316-27-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29242990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
484342
Product name
(1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine
Purity
98%
Packaging
1g
Price
$42.6
Updated
2025/07/31
TCI Chemical
Product number
A1699
Product name
(S,S)-N-(2-Amino-1,2-diphenylethyl)-p-toluenesulfonamide
Purity
>98.0%(T)
Packaging
1g
Price
$145
Updated
2025/07/31
Strem Chemicals
Product number
07-2370
Product name
(1S,2S)-(+)-N-(4-toluenesulfonyl)-1,2-diphenylethylenediamine, 98% (S,S)-TsDPEN
Packaging
500mg
Price
$64
Updated
2024/03/01
Strem Chemicals
Product number
07-2370
Product name
(1S,2S)-(+)-N-(4-toluenesulfonyl)-1,2-diphenylethylenediamine, 98% (S,S)-TsDPEN
Packaging
2g
Price
$125
Updated
2024/03/01
Strem Chemicals
Product number
07-2370
Product name
(1S,2S)-(+)-N-(4-toluenesulfonyl)-1,2-diphenylethylenediamine, 98% (S,S)-TsDPEN
Packaging
10g
Price
$431
Updated
2024/03/01
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(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine Chemical Properties,Usage,Production

Chemical Properties

White to slightly yellow crystalline powder

Uses

(1S,2S)-N-(p-Toluenesulfonyl)-1,2-diphenylethanediamine is used as a catalyst in the synthesis of keramamine C, a carboline alkaloid that is isolated from the Okinawan sponge Amphimedon sp. (1S,2S)-N-(p-Toluenesulfonyl)-1,2-diphenylethanediamine is also used as a catalyst in the synthesis of Tolvaptan (T536650), a selective oral vasopressin V2-receptor agonist that is used to treat hyponatremia.

Uses

Chiral diamine ligand for cooperative metal-Bronsted acid catalyzed greener reductive amination using hydrogen gas.

Metal-Br?nsted Acid Cooperative Catalysis for Asymmetric Reductive Amination

General Description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

Synthesis

29841-69-8

98-59-9

167316-27-0

Synthesis of Compound 2009: To a 2 L three-necked round-bottomed flask equipped with a temperature probe, magnetic stirring bar, nitrogen inlet, and constant-pressure dropping funnel was added (1S,2S)-1,2-diphenylethylenediamine (20 g, 0.094 mol) and dichloromethane (160 mL). The reaction mixture was cooled to 0-3 °C and 1 M sodium hydroxide solution (160 mL) was added slowly and dropwise while keeping the temperature below 5 °C. Subsequently, a solution of dichloromethane (320 mL) of p-toluenesulfonyl chloride (17.9 g, 0.094 mol) was added dropwise to the reaction system over a period of 2 hours. The biphasic reaction mixture was continued to be stirred at 0-5 °C for 1 h. Completion of the reaction was confirmed by thin layer chromatography (TLC, 50% ethyl acetate/heptane, UV detection). After completion of the reaction, the organic and aqueous phases were separated, and the organic phase was washed sequentially with water (2×320 mL) and saturated saline (320 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the crude product. The crude product was dissolved in toluene (200 mL) at 70-80 °C, maintained at this temperature, and heptane (300 mL) was added in batches. The resulting slurry was cooled to 20-25 °C and stirred for 1 hour, then further cooled to 0-5 °C and stirred for 10 minutes. The solid was collected by filtration and washed with a heptane solution of 50% toluene (3 x 1 bed volume) to give compound 2009 (30.24 g, 88% yield) as a white powder.

References

[1] Organic and Biomolecular Chemistry, 2011, vol. 9, # 7, p. 2505 - 2511
[2] Journal of Organic Chemistry, 2004, vol. 69, # 4, p. 1283 - 1289
[3] Patent: WO2010/120719, 2010, A1. Location in patent: Page/Page column 194; 196-197
[4] Patent: CN106496099, 2017, A. Location in patent: Paragraph 0033; 0034; 0035; 0048; 0049
[5] Organic Syntheses, 2005, vol. 82, p. 10 - 17

(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine Preparation Products And Raw materials

Raw materials

Preparation Products

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(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine Suppliers

Chengdu Likai Chiral Tech Co., LTD.
Tel
028-85247892 18980630336;
Email
zhenzhenge@lkchiralchina.com
Country
China
ProdList
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Chengdu rongchuangyiheng Biomedical Technology Co., Ltd
Tel
13438025684
Email
28296972@qq.com
Country
China
ProdList
139
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Shaoxing Zejun Pharmaceuticals Co.,Ltd
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0575-82126188 15395856318
Email
nbzjyyservice@zejunpharma.com
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China
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Shanghai Qiao Chemical Science Co., Ltd
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021-58892003
Email
info@qiaochem.com
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China
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J & K SCIENTIFIC LTD.
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18210857532; 18210857532
Fax
86-10-82849933
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jkinfo@jkchemical.com
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China
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006356688 18621169109
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86-21-61259102
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market03@meryer.com
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China
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INTATRADE GmbH
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+49 3493/605464
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+49 3493/605470
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sales@intatrade.de
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Germany
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Alfa Aesar
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400-6106006
Fax
021-67582001/03/05
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saleschina@alfa-asia.com
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China
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30123
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TCI (Shanghai) Development Co., Ltd.
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021-67121386
Fax
021-67121385
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Sales-CN@TCIchemicals.com
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China
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Beijing HwrkChemical Technology Co., Ltd
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18515581800 18501085097
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010-89508210
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sales.bj@hwrkchemical.com
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China
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View Lastest Price from (1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine 167316-27-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-09-19
Hebei shuoxi biotechnology co. LTD
Product
(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine 167316-27-0
Price
US $60.00/g
Min. Order
10g
Purity
99.8%
Supply Ability
10tons
Release date
2020-04-09
Longyan Tianhua Biological Technology Co., Ltd
Product
(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-diphenylethylenediamine 167316-27-0
Price
US $15.00/Kg/Bag
Min. Order
25Kg/Bag
Purity
99%
Supply Ability
20 Tons
Release date
2020-11-10

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  • 167316-27-0
  • C21H23N2O2S
  • CH3C6H4SO2NHCHC6H5CHC6H5NH2
  • Asymmetric Synthesis
  • Chiral Catalysts, Ligands, and Reagents
  • Hydrogenation
  • Chiral Nitrogen
  • DPEN Series
  • API intermediates
  • Asymmetric Synthesis
  • Synthetic Organic Chemistry
  • Asymmetric Synthesis
  • Chiral Catalysts, Ligands, and Reagents
  • HydrogenationChiral Building Blocks
  • Organic Building Blocks
  • Polyamines
  • organic amine