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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472907Generated: October 30, 2026

Trifluoroacetic acid → HCID 67215727, compound

https://huagongshe.com/reaction/472907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67215732HCID 67215732—
SolventDichloromethaneHCID 6344—
ProductHCID 67215727HCID 6721572797.8%

Reaction Steps

1.3 ml of trifluoroacetic acid are added to 460 mg (1.01 mmol) of methyl 5-({6-[(tert-butoxycarbonyl)-(methyl)amino]imidazo[1,5-a]pyridin-3-yl}carbonyl)-2-nitrobenzoate in 5 ml of dichloromethane and the mixture is stirred at ambient temperature overnight. The reaction medium is concentrated under reduced pressure. The residue is taken up in water and basified with a saturated aqueous sodium bicarbonate solution and then extracted with dichloromethane. The organic phase is washed with a saturated aqueous sodium chloride solution, then dried over sodium sulfate and concentrated under reduced pressure. 350 mg of a red powder are obtained. Melting point: 183° C.; 1H NMR (d6-DMSO): 2.79 (3H, d), 3.90 (3H, s), 7.11 (1H, d), 7.77 (1H, s), 7.82 (1H, d), 8.31 (1H, d), 8.66 (1H, d), 8.75 (1H, s), 9.01 (1H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633216B2
Source datasetuspto-grants-2014_01
ORD IDord-b062d6095e0a4916a5e14fc196bff003
Source noteuspto-grants-2014_01