Basic information Safety Supplier Related

2-N-BOC-AMINO-THIAZOLE-5-CARBOXYLIC ACID

Basic information Safety Supplier Related

2-N-BOC-AMINO-THIAZOLE-5-CARBOXYLIC ACID Basic information

Product Name:
2-N-BOC-AMINO-THIAZOLE-5-CARBOXYLIC ACID
Synonyms:
  • 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylic acid
  • 2-Boc-aminothiazole-5-carboxylic acid
  • 2-N-Boc-AMino-thiazole-5-carboxylicacid/2-(tert-butoxycarbonylaMino)thiazole-5-carboxylicacid
  • 5-Thiazolecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-
  • 2-(tert-Butoxycarbonylamino)thiazole-5-carboxylic Acid
  • 2-Amino-1,3-thiazole-5-carboxylic acid, N-BOC protected 97%
  • 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylic aci...
  • 2-N-Boc-Amino-thiazole-5-carboxylic acid, CAS 302964-02-9
CAS:
302964-02-9
MF:
C9H12N2O4S
MW:
244.27
Product Categories:
  • CHIRAL CHEMICALS
Mol File:
302964-02-9.mol
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2-N-BOC-AMINO-THIAZOLE-5-CARBOXYLIC ACID Chemical Properties

Melting point:
220-222°(dec)
Density 
1.406±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
powder to crystal
pka
5.53±0.70(Predicted)
color 
White to Almost white
CAS DataBase Reference
302964-02-9
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Safety Information

Hazard Codes 
Xi
Risk Statements 
43-36/37/38
Safety Statements 
36/37-36-26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29349990
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2-N-BOC-AMINO-THIAZOLE-5-CARBOXYLIC ACID Usage And Synthesis

Chemical Properties

White solid

Uses

A reactant used in the preparation of 2-aminocarboxamidothiazoles as inhibitors of Src-family kinase.

Synthesis

302964-01-8

302964-02-9

General procedure for the synthesis of 2-(tert-butoxycarbonylamino)thiazole-5-carboxylic acid from ethyl 2-(tert-butoxycarbonylamino)thiazole-5-carboxylate: To a vigorously stirred suspension of ethyl 2-(tert-butoxycarbonylamino)thiazole-5-carboxylate (4.2 g, 15 mmol) in methanol (11 mL) was slowly added an aqueous 2 M NaOH solution (22 mL, 44.0 mmol). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was concentrated under vacuum by rotary evaporator to remove methanol. The pH was adjusted to 1-2 by adding aqueous 6 N HCl dropwise to the residual aqueous suspension. the mixture was stirred for 1 h, during which time it was occasionally sonicated to promote precipitation. The resulting white solid was collected by filtration, washed thoroughly with deionized water and dried in a vacuum drying oven to afford 2-(tert-butoxycarbonylamino)thiazole-5-carboxylic acid (3.7 g, 100% yield). Mass spectrometry analysis showed (M + H-Boc)+ = 145.

References

[1] Patent: WO2009/100171, 2009, A1. Location in patent: Page/Page column 109
[2] Patent: CN106674150, 2017, A. Location in patent: Paragraph 0022-0026
[3] Patent: US2004/54186, 2004, A1. Location in patent: Page 23
[4] Synthetic Communications, 2017, vol. 47, # 17, p. 1610 - 1621
[5] Asian Journal of Chemistry, 2018, vol. 30, # 7, p. 1621 - 1628

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