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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269363Generated: November 1, 2026

Trifluoroacetic acid → HCID 70073493, compound

https://huagongshe.com/reaction/2269363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70085747HCID 70085747—
SolventDichloromethaneHCID 6344—
ProductHCID 70073493HCID 7007349398%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (2S)-6-benzyloxycarbonylamino-2-tert-butoxycarbonylaminohexanoic acid 1,3,4-thiadiazol-2-ylamide (0.81 g, 1.75 mmol) in dichloromethane (8 mL) is added trifluoroacetic acid (2 mL). The resulting solution is stirred for 4 h at 25° C., is concentrated, diluted with 50 mL of EtOAc, and washed with 1 N aqueous sodium hydroxide solution. The organic layer is dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide (2S)-6-benzyloxycarbonylamino-2-aminohexanoic acid 1,3,4-thiadiazol-2-ylamide as a solid (0.62 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329400B1
Source datasetuspto-grants-2001_12
ORD IDord-e5075a3c8fd3469483865e63ff6306e2
Source noteuspto-grants-2001_12