ChemicalBook > CAS DataBase List > (R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE

(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE

Product Name
(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE
CAS No.
143322-56-9
Chemical Name
(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE
Synonyms
InterMediate of Eletriptan;3-(N- benzyloxycarbonyl-D-prolyl)-5-bromoindole;(5R)3-(N-benzyloxycarbonyl-D-prolyl)-5-bromoindole;(R)-5-bromo-3-[(1-methyl-2-pyrrolidinyl)methyl]-1H-indole;(R)-Benzyl 2-(5-bromo-1H-indole-3-carbonyl)-pyrrolidine-1-carboxylate;(R)-(5-bromo-1H-indol-3-yl)[N-[(phenylmethoxy)carbonyl]-2-pyrrolidinyl]methanone;(R)-2-[(5-Bromo-1H-indol-3-yl)carbonyl]-1-pyrrolidinecarboxylic acid benzyl ester;(2R)-2-[(5-BroMo-1H-indol-3-yl)carbonyl]-1-pyrrolidinecarboxylic Acid PhenylMethyl Ester;1-Pyrrolidinecarboxylic acid, 2-[(5-bromo-1H-indol-3-yl)carbonyl]-, phenylmethyl ester, (R)-;1-Pyrrolidinecarboxylic acid, 2-[(5-bromo-1H-indol-3-yl)carbonyl]-, phenylmethyl ester, (2R)-
CBNumber
CB32129544
Molecular Formula
C21H19BrN2O3
Formula Weight
427.29
MOL File
143322-56-9.mol
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(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE Property

Boiling point:
605.0±55.0 °C(Predicted)
Density 
1.505
storage temp. 
2-8°C
solubility 
soluble in Dichloromethanol, Ethyl Acetate, Methanol
form 
Solid
pka
14.40±0.30(Predicted)
color 
White
CAS DataBase Reference
143322-56-9(CAS DataBase Reference)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B285927
Product name
R-3-(N-Benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-bromo-1H-indole
Packaging
250mg
Price
$1100
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18508
Product name
R-3-(N-Benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-bromo-1H-indole
Packaging
250mg
Price
$1365
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18508
Product name
R-3-(N-Benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-bromo-1H-indole
Packaging
10mg
Price
$125.1
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18508
Product name
R-3-(N-Benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-bromo-1H-indole
Packaging
25mg
Price
$227.5
Updated
2021/12/16
Matrix Scientific
Product number
096542
Product name
(R)-Benzyl 2-(5-bromo-1H-indole-3-carbonyl)-pyrrolidine-1-carboxylate
Purity
95+%
Packaging
250mg
Price
$288
Updated
2021/12/16
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(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE Chemical Properties,Usage,Production

Chemical Properties

White Solid

Synthesis

10075-50-0

61350-62-7

143322-56-9

General procedure for the synthesis of benzyl (R)-2-(5-bromo-1H-indole-3-carbonyl)pyrrolidine-1-carboxylate from 5-bromoindole and benzyl (R)-2-(chlorocarbonyl)pyrrolidine-1-carboxylate: 5-bromoindole (15.7 g, 80.4 mmol) was added to a 500 mL four-necked flask with dichloromethane (140 mL). The temperature of the reaction system was lowered to 0 °C under cooling in an ice bath, and aluminum trichloride solid (16.1 g, 120.6 mmol) was slowly added, taking care to add it in batches and controlling the internal temperature between 0 and 5 °C. After addition, the reaction was continued to be stirred at 0~5°C for 1 hour. Subsequently, a dichloromethane solution of N-benzyloxycarbonyl prolyl chloride prepared in Example 1 was slowly added dropwise under the same temperature conditions. After the dropwise addition was completed, the reaction was continued to be stirred for 6 hours by keeping 0~5°C. At the end of the reaction, the reaction system was placed in an ice bath and the reaction was quenched by slowly dropping 90 mL of saturated ammonium chloride solution. The reaction mixture was filtered, the filtrate was separated and the organic phase was washed with saturated sodium bicarbonate solution and saturated brine sequentially. After the solvent was removed by concentration under reduced pressure, the resulting crude product was purified by recrystallization using a solvent mixture of ethyl acetate and n-heptane (1:1, v/v). The purified product was dried under vacuum at 60 °C for 8 h to afford (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-bromo-1H-indole (14.2 g) as a white solid in 83% yield and 99.2% HPLC purity.

References

[1] Patent: CN104230895, 2017, B. Location in patent: Paragraph 0031; 0032; 0033; 0034; 0035; 0036-0044
[2] Medicinal Chemistry Research, 1999, vol. 9, # 9, p. 668 - 674
[3] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 20, p. 3419 - 3421
[4] Patent: US2008/319205, 2008, A1. Location in patent: Page/Page column 7
[5] Patent: US2011/166364, 2011, A1. Location in patent: Page/Page column 4

(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE Suppliers

AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
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60
Matrix Scientific
Tel
--
Fax
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Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
NE Scientific
Tel
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United States
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5030
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View Lastest Price from (R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE manufacturers

Career Henan Chemical Co
Product
(R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLE 143322-56-9
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200kgs
Release date
2020-01-28

143322-56-9, (R)-5-BROMO-3-[(1-METHYL-2-PYRROLIDINYL)METHYL]-1H-INDOLERelated Search:


  • (R)-5-bromo-3-[(1-methyl-2-pyrrolidinyl)methyl]-1H-indole
  • (R)-2-[(5-Bromo-1H-indol-3-yl)carbonyl]-1-pyrrolidinecarboxylic acid benzyl ester
  • (2R)-2-[(5-BroMo-1H-indol-3-yl)carbonyl]-1-pyrrolidinecarboxylic Acid PhenylMethyl Ester
  • InterMediate of Eletriptan
  • (R)-Benzyl 2-(5-bromo-1H-indole-3-carbonyl)-pyrrolidine-1-carboxylate
  • 1-Pyrrolidinecarboxylic acid, 2-[(5-bromo-1H-indol-3-yl)carbonyl]-, phenylmethyl ester, (R)-
  • 1-Pyrrolidinecarboxylic acid, 2-[(5-bromo-1H-indol-3-yl)carbonyl]-, phenylmethyl ester, (2R)-
  • (R)-(5-bromo-1H-indol-3-yl)[N-[(phenylmethoxy)carbonyl]-2-pyrrolidinyl]methanone
  • 3-(N- benzyloxycarbonyl-D-prolyl)-5-bromoindole
  • (5R)3-(N-benzyloxycarbonyl-D-prolyl)-5-bromoindole
  • 143322-56-9
  • 163322-57-0
  • Chiral Reagents
  • Indole Derivatives
  • Intermediates & Fine Chemicals
  • Pharmaceuticals