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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32815Generated: October 25, 2026

4-Methylmorpholine → tert-Butyl (4-(methoxy(methyl)carbamoyl)thiazol-2-yl)carbamate

https://huagongshe.com/reaction/32815

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-4,6-dimethoxy-1,3,5-triazineHCID 18450—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant2-Amino-1,3-thiazole-4-carboxylic acid, N-BOC protectedHCID 1502051—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (4-(methoxy(methyl)carbamoyl)thiazol-2-yl)carbamateHCID 5860431488,069.203%

Reaction Steps

A solution of 2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid (14 g, 0.0573 mol), 2-chloro-4,6-dimethoxy-1,3,5-triazine (10.06 g, 0.0573 mol) and N-methyl morpholine (5.79 g, 0.0573 mol) in tetrahydrofuran was stirred for 2 hours at room temperature. N,O-Dimethylhydroxylamine hydrochloride (5.59 g, 0.0573 mmol) and triethylamine (5.59 g, 0.0573 mol) were added and the mixture was stirred for 3 days. The reaction mixture was evaporated and ethyl acetate was added. The reaction mixture was washed with 1 N aqueous hydrochloric acid and then washed with saturated aqueous sodium bicarbonate. [4-(Methoxy-methyl-carbamoyl)-thiazol-2-yl]-carbamic acid tert-butyl ester (14.5 g, 88%) was obtained as a tan tar after drying (magnesium sulfate) and evaporation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427635B2
Source datasetuspto-grants-2008_09
ORD IDord-59be9c7ae1d246e5bf7b527b4f99c272
Source noteuspto-grants-2008_09