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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522981Generated: October 29, 2026

Trifluoroacetic acid → HCID 73058384, compound

https://huagongshe.com/reaction/522981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131735558HCID 131735558—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 73058384HCID 7305838478.4%

Reaction Steps

To a solution of N-tert-butyl-2-(3-methylisothiazol-5-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (32 mg, 69.5 mol) in dichloromethane (1.2 mL) was added trifluoroacetic acid (158 mg, 107 μL, 1.39 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 (1.2 mL), methanol (0.6 mL) and ammonium hydroxide (0.15 mL) and stirred at room temperature for 2 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-(3-methylisothiazol-5-ylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (18 mg, 54.5 mol, 78.4%) as a brown solid. 1H NMR (400 MHz, DMSO-d) δ ppm: 12.55 (s, 1H), 11.39 (s, 1H), 8.15 (d, J=3.2, 1 H), 8.11 (s, 1H), 7.37 (s, 1H), 6.70 (s, 1H), 2.33 (s, 3H), 1.55 (s, 9H); MS (EI/CI) m/z: 331.1 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334278B2
Source datasetuspto-grants-2016_05
ORD IDord-a9cb60912a6f4b8ab30696fd902cffa2
Source noteuspto-grants-2016_05