ChemicalBook--->CAS DataBase List--->1094070-77-5

1094070-77-5

1094070-77-5 Structure

1094070-77-5 Structure
IdentificationBack Directory
[Name]

tert-butyl 2-bromothiazol-5-ylcarbamate
[CAS]

1094070-77-5
[Synonyms]

5-(Boc-aMino)-2-broMothiazole
tert-Butyl (2-bromothiazol-5-yl)
tert-butyl 2-bromothiazol-5-ylcarbamate
tert-Butyl N-(2-broMo-5-thiazolyl)carbaMate
tert-butyl N-(2-bromo-1,3-thiazol-5-yl)carbamate
(2-BroMo-thiazol-5-yl)-carbaMic acidtert-butyleste
(2-Bromo-thiazol-5-yl)-carbamicacidtert-butylester
N-(2-Bromo-5-thiazolyl)carbamic acid tert-butyl ester
tert-butyl 2-bromothiazol-5-ylcarbamate ISO 9001:2015 REACH
Carbamic acid, N-(2-bromo-5-thiazolyl)-, 1,1-dimethylethyl ester
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C8H11BrN2O2S
[MDL Number]

MFCD13195442
[MOL File]

1094070-77-5.mol
[Molecular Weight]

279.15
Chemical PropertiesBack Directory
[Boiling point ]

294℃
[density ]

1.574
[Fp ]

131℃
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

11.83±0.70(Predicted)
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C8H11BrN2O2S/c1-8(2,3)13-7(12)11-5-4-10-6(9)14-5/h4H,1-3H3,(H,11,12)
[InChIKey]

DXTQRJCFSNCPMD-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)NC1SC(Br)=NC=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H302-H335
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

tert-Butyl (2-bromothiazol-5-yl)carbamate is a useful reactant for the synthesis of imidazo[1,2-a]pyrazine deratives, which could act as Aurora kinase inhibitors.
[Synthesis]

2-Bromo-5-thiazolecarboxylic acid

54045-76-0

tert-Butanol

75-65-0

tert-butyl 2-bromothiazol-5-ylcarbamate

1094070-77-5

Synthesis of tert-butyl 2-bromothiazole-5-carbamate: 2-bromothiazole-5-carboxylic acid (2.29 g, 11.0 mmol) was added to a 250 mL round bottom flask and ground to a fine powder using a spatula. Tert-butanol (12.2 mL, 11.0 mmol) and triethylamine (TEA, 1.53 mL, 11.0 mmol) were then added and rapid dissolution of the solid was observed. Diphenylphosphoryl azide (DPPA, 2.61 mL, 12.1 mmol) was then added, and the flask was sealed with a rubber septum and the sealed flask was heated in an 80 °C oil bath. After 10 hours of reaction, the reaction mixture was transferred to a partition funnel and extracted with saturated saline (100 mL) and ethyl acetate (EtOAc, 100 mL). The organic layer was separated and dried over anhydrous sodium sulfate. The dried organic phase was concentrated onto silica gel and purified by rapid column chromatography on a Redi-Sep? pre-populated silica gel column (120 g) using a gradient elution of 0% to 80% ethyl acetate in hexane. The final target product, tert-butyl 2-bromothiazole-5-carbamate (2.02 g, 66% yield), was obtained as an off-white crystalline solid. It was analyzed by LCMS (API-ES) and measured m/z (relative abundance): 279 (100%, [M-H]-).

[References]

[1] Patent: WO2009/11880, 2009, A2. Location in patent: Page/Page column 138-139
[2] Patent: WO2013/186089, 2013, A2. Location in patent: Page/Page column 94; 95
[3] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 5, p. 1559 - 1564
Spectrum DetailBack Directory
[Spectrum Detail]

tert-butyl 2-bromothiazol-5-ylcarbamate(1094070-77-5)1HNMR
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