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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582911Generated: November 2, 2026

Trifluoroacetic anhydride → HCID 21866517, compound

https://huagongshe.com/reaction/1582911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantDiisopropylethylamineHCID 81531—
ReactantCarbamic acid, [[5-(aminocarbonyl)-4-methyl-2-thiazolyl]methyl]-, 1,1-dimethylethyl esterHCID 21866488—
SolventDichloromethaneHCID 6344—
ProductHCID 21866517HCID 21866517—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(N-BOC-Aminomethyl)-4-methylthiazole-5-carboxamide [sic] (11.13 g, 41.02 mmol) was suspended in dichloromethane (75 ml) and cooled to 0° C. At this temperature, ethyldiisopropylamine (17.86 ml, 102.55 mmol) was first added, and then, slowly, a solution of trifluoroacetic anhydride (6.56 ml, 47.17 mmol) in dichloromethane (20 ml). After stirring for 1 hour, the mixture was diluted with dichloromethane and washed with 5% strength citric acid solution. After drying (MgSO4), the solvent was removed on a rotary evaporator and the crude product was purified by flash chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740647B1
Source datasetuspto-grants-2004_05
ORD IDord-e3233e3658a647299ea0e7f30be7437b
Source noteuspto-grants-2004_05