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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174877Generated: November 1, 2026

Trifluoroacetic acid → HCID 11548026, compound

https://huagongshe.com/reaction/1174877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59557927HCID 59557927—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11548026HCID 1154802620%

Reaction Steps

To a solution of {[4-(3-tert-butyl-5-{3-[4-(pyridin-4-yloxy)-phenyl]-ureido}-pyrazol-1-yl)-benzylcarbamoyl]-methyl}-carbamic acid tert-butyl ester (60 mg, 0.10 mmol) in THF (5 mL) was added TFA (3 mL), and the resulting mixture was stirred at room temperature for 18 h. The reaction mixture was partitioned between EtOAc (20 mL) and saturated NaHCO3 aqueous solution (20 mL), and the organic layer was removed and washed with brine, dried over Na2SO4, and concentrated at reduced pressure. The residue was purified by preparative TLC (90:10 CH2Cl2/MeOH) to give 10 mg (20%) of the desired product. 1H-NMR (DMSO-d6) δ 8.72 (s, 1H), 8.32 (d, J=5.7 Hz, 2H), 8.02 (s, 1H), 7.53 to 7.30 (m, 6H), 6.96 (d, J=6.6 Hz, 2H), 6.73 (d, J=6.3 Hz, 2H), 6.32 (s, 1H), 4.36 (s, 2H), 3.70 (S, 2H), 1.18 (s, 9H); MS LC-MS [M+H]+=513, RT=2.01 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838524B2
Source datasetuspto-grants-2010_11
ORD IDord-9f418d9dd47f4b398381fb619db70a03
Source noteuspto-grants-2010_11