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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446949Generated: October 29, 2026

(S)-tert-butyl 2-(2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamido)propanoate → (S)-2-(2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamido)propanoic acid

https://huagongshe.com/reaction/446949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 2-(2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamido)propanoateHCID 67388507—
Solvent2,2,2-TrifluoroethanolHCID 6409—
Product(S)-2-(2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamido)propanoic acidHCID 6738789698%

Reaction Steps

A solution of (S)-tert-butyl 2-(2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamido)propanoate (265 mg, 0.58 mmol) in 2,2,2-trifluoroethanol (4 mL) was heated at 150° C. for 3 h under microwave assisted conditions. The solvent was removed under vacuum to give 230 mg (98%) of (S)-2-(2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamido)propanoic acid as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481541B2
Source datasetuspto-grants-2013_07
ORD IDord-7645b1e4253046bda7e840cac16fe5b2
Source noteuspto-grants-2013_07