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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522983Generated: October 29, 2026

Trifluoroacetic acid → HCID 73295613, compound

https://huagongshe.com/reaction/522983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131735559HCID 131735559—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 73295613HCID 7329561312%

Reaction Steps

To a solution of N-tert-butyl-2-(2,4-dimethylphenylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (82 mg, 175 mol) in dichloromethane (2.7 mL) was added trifluoroacetic acid (400 mg, 270 μL, 3.51 mmol) and the mixture stirred at room temperature for 16 h. The reaction mixture was concentrated in vacuo and the residue obtained diluted with dichloromethane (3 mL), methanol (1.5 mL) and ammonium hydroxide (0.4 mL) and stirred at room temperature for 1 h. The mixture was concentrated and triturated with water. The solid was collected by filtration and washed with water and ether to give N-tert-butyl-2-(2,4-dimethylphenylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (7 mg, 20.7 mol, 12%) as a yellow solid. 1H NMR (400 MHz, CDCl3-d) δ ppm: 9.19 (s, 1H), 8.12 (d, J=3.0, 1 H), 7.95 (s, 1H), 7.86 (s, 1H), 7.50 (d, J=7.8, 1 H), 7.15 (s, 1H), 7.08 (d, J=8.2, 1 H), 6.33 (s, 1H), 2.38 (s, 3H), 2.34 (s, 1H), 1.49 (s, 9H); MS (EI/CI) m/z: 338.2 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334278B2
Source datasetuspto-grants-2016_05
ORD IDord-e858ed8077c148d7b2b329975cb14b50
Source noteuspto-grants-2016_05