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850429-62-8

850429-62-8 Structure

850429-62-8 Structure
IdentificationBack Directory
[Name]

2-TERT-BUTOXYCARBONYLAMINOTHIAZOLE-4-CARBOXYLIC ACID METHYL ESTER
[CAS]

850429-62-8
[Synonyms]

Methyl 2-amino-1
METHYL 2-(BOC-AMINO)-4-THIAZOLECARBOXYLATE
METHYL 2-(BOC-AMINO)THIAZOLE-4-CARBOXYLATE
N-BOC-METHYL 2-AMINO-1,3-THIAZOLE-4-CARBOXYLATE
BOC-2-AMINO-4-THIAZOLE-CARBOXYLIC ACID METHYL ESTER
METHYL 2-(TERT-BUTOXYCARBONYLAMINO)THIAZOLE-4-CARBOXYLATE
METHYL 2-AMINO-1,3-THIAZOLE-4-CARBOXYLATE, N-BOC PROTECTED
Methyl 2-amino-1,3-thiazole-4-carboxylate, 2-BOC protected
Methyl 2-amino-1,3-thiazole-4-carboxylate, 2-BOC protected 98%
Methyl 2-amino-1,3-thiazole-4-carboxylate, N-BOC protected 98%
methyl 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-4-carboxy...
2-TERT-BUTOXYCARBONYLAMINOTHIAZOLE-4-CARBOXYLIC ACID METHYL ESTER
Methyl 2-{[(tert-butoxy)carbonyl]aMino}-1,3-thiazole-4-carboxylate
4-Thiazolecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-4-thiazolecarboxylic acid methyl ester
2-[(tert-Butoxycarbonyl)amino]-4-(methoxycarbonyl)-1,3-thiazole, Methyl 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-4-carboxylate
[Molecular Formula]

C10H14N2O4S
[MDL Number]

MFCD06659910
[MOL File]

850429-62-8.mol
[Molecular Weight]

258.29
Chemical PropertiesBack Directory
[Melting point ]

156-160
[storage temp. ]

2-8°C
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C10H14N2O4S/c1-10(2,3)16-9(14)12-8-11-6(5-17-8)7(13)15-4/h5H,1-4H3,(H,11,12,14)
[InChIKey]

VLJAUDDGOCGHFB-UHFFFAOYSA-N
[SMILES]

S1C=C(C(OC)=O)N=C1NC(OC(C)(C)C)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312+P330-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2934100090
Hazard InformationBack Directory
[Uses]

N-Boc Methyl 2-Aminothioazole-4-carboxylate a thiazolopyrimidinone derivative used as a modulator of NMDA receptor activity. Also a potential antiviral agent.
[Synthesis]

Methyl 2-Aminothiazole-4-carboxylate

118452-04-3

Di-tert-butyl dicarbonate

24424-99-5

2-TERT-BUTOXYCARBONYLAMINOTHIAZOLE-4-CARBOXYLIC ACID METHYL ESTER

850429-62-8

General procedure for the synthesis of methyl 2-(Boc-amino)thiazole-4-carboxylate from methyl 2-aminothiazole-4-carboxylate and di-tert-butyl dicarbonate: to a 1:1 dichloromethane/tetrahydrofuran (200mL) solution containing methyl 2-aminothiazole-4-carboxylate (10.0g, 63.22mmol, prepared as described in Example 3, Step 2), was added di-tert-butyl dicarbonate butyl ester (15.2 g, 69.64 mmol) and 4-(dimethylamino)pyridine (1.5 g, 12.30 mmol). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the mixture was partitioned between ethyl acetate and 10% w/v citric acid aqueous solution. The organic layer was separated, washed sequentially with water and brine, and then dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the crude product was purified by silica gel column chromatography to afford methyl 2-(tert-butoxycarbonylamino)thiazole-4-carboxylate as an oil (15.5 g, 95% yield) using 2:3 ethyl acetate/hexane as eluent.

[References]

[1] Patent: US2006/63814, 2006, A1. Location in patent: Page/Page column 61
[2] Patent: WO2015/52226, 2015, A1. Location in patent: Paragraph 0487
[3] Patent: WO2014/37480, 2014, A1. Location in patent: Page/Page column 125; 126
Spectrum DetailBack Directory
[Spectrum Detail]

2-TERT-BUTOXYCARBONYLAMINOTHIAZOLE-4-CARBOXYLIC ACID METHYL ESTER(850429-62-8)1HNMR
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