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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403359Generated: October 30, 2026

Trifluoroacetic acid → HCID 70984185, compound

https://huagongshe.com/reaction/403359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70984156HCID 70984156—
SolventDichloromethaneHCID 6344—
ProductHCID 70984185HCID 7098418590%

Reaction Steps

(4R,7S,8S)-8-(tert-butoxycarbonylamino)-7-(2,3-difluorophenyl)-2-(trifluoromethyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazol-4-yl 4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxylate (3.5 mg, 4.94 μmol) in methylene chloride (2 mL) was treated with trifluoroacetic acid (0.5 mL, 6.49 mmol) at rt. The reaction was stirred for 2 h. The solvent was removed under vacuum and the crude product was partitioned between sodium bicarbonate(sat.) and ethyl acetate. The organic layer was separated, dried (sodium sulfate), filtered and concentrated in vacuo. Flash chromatography, eluting with methanol in methylene chloride from 0 to 10% gave the desired product (2.7 mg, 90%) as a white solid: LCMS (M+Na=631.04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748429B2
Source datasetuspto-grants-2014_06
ORD IDord-84eb3116d0a447b0a4ad5286226bf366
Source noteuspto-grants-2014_06