Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Amides >  2-bromo-N-isopropylacetamide

2-bromo-N-isopropylacetamide

Basic information Safety Supplier Related

2-bromo-N-isopropylacetamide Basic information

Product Name:
2-bromo-N-isopropylacetamide
Synonyms:
  • 2-bromo-N-isopropylacetamide
  • 2-bromo-N-isopropylacetamide(SALTDATA: FREE)
  • acetamide, 2-bromo-N-(1-methylethyl)-
  • 2-bromo-N-isopropylacetamide in stock Factory
  • 2-Bromo-N-(1-methylethyl)-acetamide
  • N-(Bromoacetyl)isopropylamine
  • 2-broMo-N-(propan-2-yl)acetaMide
  • Belumosudil Impurity 8
CAS:
75726-96-4
MF:
C5H10BrNO
MW:
180.04
Mol File:
75726-96-4.mol
More
Less

2-bromo-N-isopropylacetamide Chemical Properties

Melting point:
63-64℃
Boiling point:
266℃
Density 
1.378
Flash point:
115℃
storage temp. 
Inert atmosphere,Room Temperature
pka
13.71±0.46(Predicted)
InChI
InChI=1S/C5H10BrNO/c1-4(2)7-5(8)3-6/h4H,3H2,1-2H3,(H,7,8)
InChIKey
ZLDCRYWMEQJDGW-UHFFFAOYSA-N
SMILES
C(NC(C)C)(=O)CBr
More
Less

Safety Information

HazardClass 
IRRITANT
HS Code 
2924297099
More
Less

2-bromo-N-isopropylacetamide Usage And Synthesis

Uses

2-Bromo-N-isopropylacetamide is a an intermediate of Belumosudil.

Synthesis

75-31-0

598-21-0

75726-96-4

Dichloromethane (5 mL) and isopropylamine (1.2 mmol) were added to a 25 mL round-bottomed flask, corked tightly and protected under a nitrogen atmosphere. Bromoacetyl bromide (1 mmol) was slowly added dropwise over 2 min under ice bath cooling and stirring conditions. After the dropwise addition, the reaction was continued in an ice bath for 5 min, after which the reaction mixture was transferred to room temperature and stirred for 1 hr. The progress of the reaction was monitored by thin layer chromatography (TLC) until the complete disappearance of bromoacetyl bromide. Upon completion of the reaction, the resulting white solid was collected by filtration and washed with dichloromethane. The filtrate and washings were combined, and the organic layer was sequentially extracted with dilute hydrochloric acid solution, dichloromethane, washed with saturated brine and dried with anhydrous Na2SO4. After concentration under reduced pressure to remove the solvent, the target compound 2-bromo-N-isopropylacetamide was purified by column chromatography to afford the target compound as a white solid in 71% yield.

References

[1] Journal of the American Chemical Society, 2006, vol. 128, # 48, p. 15476 - 15489
[2] Patent: CN106916145, 2017, A. Location in patent: Paragraph 0017; 0035-0038; 0058; 0066
[3] Patent: WO2008/54599, 2008, A2. Location in patent: Page/Page column 152
[4] Patent: WO2010/104851, 2010, A1. Location in patent: Page/Page column 147; 148
[5] Patent: WO2014/55999, 2014, A2. Location in patent: Paragraph 0164

2-bromo-N-isopropylacetamideSupplier

Shandong Xuanshuo Pharmaceutical Technology Co. LTD Gold
Tel
15269103900
Email
suchangzhou@shiningpharm.com
Nantong Xiaochang Pharmaceutical Trading Co., Ltd. Gold
Tel
0513-82104991 18912868361
Email
sales11@btcpharm.com
Nanjing Winsome Chemical Limited Gold
Tel
025-84651981 18652010011
Email
sales@nastchem.com
Shandong Shining Pharm Co.,Ltd Gold
Tel
18866891188
Email
zhaojiangxia@shiningpharm.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com