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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362644Generated: October 31, 2026

Trifluoroacetic acid → HCID 67003382, compound

https://huagongshe.com/reaction/2362644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67003555HCID 67003555—
SolventDichloromethaneHCID 6344—
ProductHCID 67003382HCID 67003382—

Reaction Steps

To an ambient solution of 5-(5-chloro-2-(1-(2-(pyrrolidin-1-yl)ethyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-2-(3-(4-methoxybenzyloxy)oxetan-3-yl)thiazole (Example 20B) (160 mg, 0.215 mmol) in dichloromethane (2.5 mL) was added trifluoroacetic acid (2.5 mL, 32.4 mmol). The reaction was stirred for 0.5 hours and then concentrated to dryness under reduced pressure. The residue was partitioned between ethyl acetate (5 mL) and saturated aqueous bicarbonate solution (1 mL). The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with 0 to 10% methanol in dichloromethane, to give the title compound. MS ESI(+) m/z 625.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691810B2
Source datasetuspto-grants-2014_04
ORD IDord-e5ff7aea933044e983f887982bb20154
Source noteuspto-grants-2014_04