HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582911Generated: November 2, 2026
Trifluoroacetic anhydride → HCID 21866517, compound
https://huagongshe.com/reaction/1582911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Carbamic acid, [[5-(aminocarbonyl)-4-methyl-2-thiazolyl]methyl]-, 1,1-dimethylethyl ester | HCID 21866488 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21866517 | HCID 21866517 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740647B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-e3233e3658a647299ea0e7f30be7437b |
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| Source note | uspto-grants-2004_05 |
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