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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424180Generated: November 3, 2026

Trifluoroacetic acid → HCID 86699098, compound

https://huagongshe.com/reaction/1424180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86699115HCID 86699115—
SolventDichloromethaneHCID 6344—
ProductHCID 86699098HCID 86699098102.3%

Reaction Steps

tert-Butyl((1S,2R)-3-amino-1-(6-(tert-butyl)imidazo[1,2-a]pyridin-2-yl)-2-methyl-3-oxopropyl)carbamate (Preparation 37, 311 mg) was dissolved in dichloromethane (ca 4 mL) and excess trifluoroacetic acid (ca 0.5 mL) was added. The reaction mixture was stirred for 18 hours then the solvent was removed in vacuo. The residue was dissolved in dichloromethane and washed with saturated aqueous sodium bicarbonate. The product stayed in the aqueous phase. The aqueous phase was adjusted to pH=10 with 1N sodium hydroxide, then sodium chloride was added until the solution was saturated. The aqueous phase was extracted three times with ethyl acetate. The combined organic phase was dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The residue was purified by silica gel column chromatography eluting with 0-100% CMA80 in dichloromethane to afford 233 mg of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927587B2
Source datasetuspto-grants-2015_01
ORD IDord-63665a8283ac45f3a5afd9e6f92e1ac8
Source noteuspto-grants-2015_01