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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114575Generated: October 30, 2026

Trifluoroacetic acid → HCID 178486158, compound

https://huagongshe.com/reaction/2114575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68877139HCID 68877139—
SolventChloroformHCID 6212—
ProductHCID 178486158HCID 17848615877.9%

Reaction Steps

C-[3-(2-Chloro-phenyl)-6-(2,4-difluoro-phenoxy)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]-N,N-dimethyl-methanesulfonamide (273 mg, 0.447 mmol) was dissolved in 5 mL chloroform, and 2.5 mL of trifluoroacetic acid was added. The reaction mixture was stirred for 22 hours at room temperature, and was then concentrated to dryness under reduced pressure. The residue was dissolved in 7 mL of MeOH, and sodium borohydride (109 mg, 4.47 mmol) was added. The reaction mixture was stirred for 15 minutes, then concentrated under reduced pressure. The residue was partitioned between 100 mL EtOAc and 100 mL brine, and the organic layer was separated, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified via flash chromatography (0% to 40% EtOAc in hexanes) to yield 167 mg of C-[3-(2-Chloro-phenyl)-6-(2,4-difluoro-phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]-N,N-dimethyl-methanesulfonamide. Mass Spec. M+H=481.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435731B2
Source datasetuspto-grants-2008_10
ORD IDord-7c4d67e45c9340a4900940e7b2ef3bb6
Source noteuspto-grants-2008_10