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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487334Generated: October 31, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/1487334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89995501HCID 89995501—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 642279%
ProductHCID 89995502HCID 89995502—

Reaction Steps

A solution of (3S,4S)-tert-butyl 3-((7-carbamoyl-2-(1-ethyl-1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-8-yl)amino)-4-(fluoromethyl)pyrrolidine-1-carboxylate (15 mg, 0.032 mmol) in DCM (0.5 ml) was treated with TFA (0.024 ml, 0.317 mmol) at room temperature for 2 h. The reaction mixture was concentrated to give 2-(1-ethyl-1H-pyrazol-4-yl)-8-(((3S,4S)-4-(fluoromethyl)pyrrolidin-3-yl)amino)imidazo[1,2-b]pyridazine-7-carboxamide, 2 TFA (15.1 mg, 0.025 mmol, 79% yield) as a white solid. ESI-MS (Method A): m/z 373.3 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428511B2
Source datasetuspto-grants-2016_08
ORD IDord-be8b4c4f91a24557940d20a682977260
Source noteuspto-grants-2016_08