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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173298Generated: October 31, 2026

Triethylamine → HCID 67517382, compound

https://huagongshe.com/reaction/2173298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 67518270HCID 67518270—
SolventDichloromethaneHCID 6344—
ProductHCID 67517382HCID 6751738287%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tert-butyl 4-[(7-carbamoyl-2,3-dihydro-1-benzofuran-3-yl)methyl]piperazine-1-carboxylate in DCM (80 mg, 0.22 rnmol) was added Et3N (60 mg, 0.59 mmol). The solution was cooled to 0° C. and TFAA (60 mg, 0.29 mmol) was added dropwise under nitrogen. After 4 hours stirring at room temperature, the solvents were removed under vacuum to give the crude product tert-butyl 4-[(7-cyano-2,3-dihydro-1-benzofuran-3-yl)methyl]piperazine-1-carboxylate (66 g, yield 87%) which was used for next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-cb4d1ab874574658ab5c40eea6c9f270
Source noteuspto-grants-2015_06