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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423164Generated: November 3, 2026

Trifluoroacetic acid → HCID 67240357, compound

https://huagongshe.com/reaction/2423164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantSodium hydrideHCID 24758—
ReactantHCID 69036330HCID 69036330—
SolventDimethylformamideHCID 6228—
ProductHCID 67240357HCID 67240357—

Reaction Conditions

Temperature50 °C

Reaction Steps

tert-Butyl 10-chloro-1,3,4,8-tetrahydro-2H-[1,4]oxazepino[6,7-e]indole-2-carboxylate (Intermediate 20, 10 mg, 0.031 mmol) was dissolved in dry DMF (1 mL) and sodium hydride (60% in mineral oil, 2.5 mg, 0.062 mmol) was added all in one portion. The mixture was stirred for 10 minutes at room temperature before 4-fluorobenzenesulfonyl chloride (12 mg, 0.062 mmol) was added. The reaction mixture was stirred for 10 minutes, and TFA (1 mL) was added dropwise. The reaction mixture was heated at 50° C. overnight and evaporated. The crude material was purified by preparative HPLC (ACE C8, 0.1% TFA-CH3CN) to give the title compound as a white solid (9.8 mg) in the form of the trifluoroacetate salt. MS m/z 381 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960374B2
Source datasetuspto-grants-2011_06
ORD IDord-c150366133e049b08af339192b1509a2
Source noteuspto-grants-2011_06