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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842614Generated: November 4, 2026

Trifluoroacetic acid → HCID 86692130, compound

https://huagongshe.com/reaction/1842614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89752097HCID 89752097—
SolventDichloromethaneHCID 6344—
ProductHCID 86692130HCID 8669213082.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

tert-Butyl{(1R,2R)-2-[({5-ethyl-4-[6-(2,2,2-trifluoroethoxy)pyrazolo[1,5-a]pyrimidin-3-yl]thiophen-2-yl}carbonyl)amino]-3,3-difluorocyclohexyl}carbamate (34.0 mg, 0.056 mmol) was dissolved in dichloromethane (1.0 mL) and trifluoroacetic acid (0.100 mL, 1.30 mmol) was added. The reaction was stirred at 40° C. for 2 h. The reaction mixture was quenched with 1N KOH in MeOH and concentrated under reduced pressure. The residue was mixed with water and extracted 3× with dichloromethane. The organic layers were combined, dried with sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (0-20% MeOH/DCM) to give the title compound (23.0 mg, 0.046 mmol). LRMS (APCI) calc'd for (C21H22F5N5O2S) [M+H]+, 504.1; found 504.0. 1H NMR (CDCl3, 500 MHz) δ 8.48 (s, 1H), 8.37 (s, 1H), 8.15 (s, 1H), 7.88 (s, 1H), 7.03 (s, 1H), 4.52 (m, 1H), 4.43 (d, J=7.8, 2H), 3.36 (s, 1H), 2.96 (q, J=7.2, 2H), 2.17 (s, 1H), 1.48-2.02 (m, 5H), 1.33 (t, J=7.3, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946237B2
Source datasetuspto-grants-2015_02
ORD IDord-9d639d36e33447378f0b9c422b300d56
Source noteuspto-grants-2015_02