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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246493Generated: October 30, 2026

Trifluoroacetic acid → HCID 71280294, compound

https://huagongshe.com/reaction/246493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 71280657HCID 71280657—
SolventDichloromethaneHCID 6344—
ProductHCID 71280294HCID 7128029426.1%

Reaction Steps

To a stirred solution of N-tert-butyl-2-(5-methyl-1H-indazol-1-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (0.1 g, 209 μmol) in dichloromethane (3 mL) was added trifluoroacetic acid (1 mL). After 15 h, the mixture was concentrated in vacuo then 25 mL of a Jan. 10, 1960 mixture of ammonium hydroxide/methanol/dichloromethane added. After 1 h the mixture was concentrated in vacuo. Purification by chromatography (silica, 24 g Analogix column, 0-4% methanol containing 10% ammonium hydroxide in dichloromethane) gave 2-(5-methyl-indazol-1-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid tert-butylamide (19 mg, 26%). MS (M+H)+=349; 1H NMR (DMSO-d6) δ: 9.03 (s, 1H), 8.49 (d, J=8.5 Hz, 1H), 8.43-8.46 (m, 2H), 8.39 (d, J=3.0 Hz, 1H), 7.73 (s, 1H), 7.65 (s, 1H), 2.48 (br. s., 3H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-e676134958b246d9ad0ef6569ab1f579
Source noteuspto-grants-2014_02