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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405688Generated: October 28, 2026

Triethylamine → Methyl 2-(2-((tert-butoxycarbonylamino)methyl)thiazole-4-carboxamido)-2-methylpropanoate

https://huagongshe.com/reaction/405688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-(((Tert-butoxycarbonyl)amino)methyl)thiazole-4-carboxylic acidHCID 10199046—
ReactantMethyl 2-aminoisobutyrate hydrochlorideHCID 13258034—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(2-((tert-butoxycarbonylamino)methyl)thiazole-4-carboxamido)-2-methylpropanoateHCID 6799199287%

Reaction Steps

To a round bottom flask with 50 mL methylene chloride was added 2-((tert-butoxycarbonylamino)methyl)thiazole-4-carboxylic acid (2.0 g, 7.74 mmole) and methyl 2-amino-2-methylpropanoate hydrochloride salt (1.25 g, 8.13 mmole). To the mixture, triethylamine (5.4 mL, 38.7 mmole) was then added, followed by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (2.97 g, 15.5 mmole) and hydroxybenzotriazole (2.09 g, 15.5 mmole). The resulting mixture was stirred at room temperature overnight. The mixture was then diluted with methylene chloride. The mixture was then washed with water and the aqueous layer was extracted with methylene chloride. The combined organic layer was then dried over Na2SO4 and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 1:1 EtOAc/hexane to provide the desired product (2.40 g, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754050B2
Source datasetuspto-grants-2014_06
ORD IDord-3f960c7c1d83479e8a72bbcf461efd2b
Source noteuspto-grants-2014_06