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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677483Generated: November 2, 2026

1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → 4-(4-{3-[7-(1-Methyl-cyclohexanecarbonyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-phenyl}-piperazine-1-carbonyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1677483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
Reactant(1-methyl-cyclohexyl)-[2-(3-piperazin-1-yl-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-methanoneHCID 59540704—
Product4-(4-{3-[7-(1-Methyl-cyclohexanecarbonyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-phenyl}-piperazine-1-carbonyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 59540970—

Reaction Steps

4-(4-{3-[7-(1-Methyl-cyclohexanecarbonyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-phenyl}-piperazine-1-carbonyl)-piperidine-1-carboxylic acid tert-butyl ester was prepared starting from (1-methyl-cyclohexyl)-[2-(3-piperazin-1-yl-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-methanone and piperidine-1,4-dicarboxylic acid mono-tert-butyl ester following general procedures as described in these Examples. M+H=615.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008298B2
Source datasetuspto-grants-2011_08
ORD IDord-2119cd48e40f4a18aa289762acdf542e
Source noteuspto-grants-2011_08