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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411580Generated: October 31, 2026

tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate → (3S)-tert-Butyl 4-(6-Aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1411580

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 11737525—
Reactanttert-butyl (3S)-3-methyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 86683728—
Product(3S)-tert-Butyl 4-(6-Aminopyridin-3-yl)-3-methylpiperazine-1-carboxylateHCID 8668373096%

Reaction Steps

Following the procedures as described for compound 101h, hydrogenation of 130a (5.8 g) afforded 130b as a brown solid (4.9 g, 96%). LCMS: [M+H]+ 293

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921353B2
Source datasetuspto-grants-2014_12
ORD IDord-34c869a2b35c43aeaf72129bc00e5e81
Source noteuspto-grants-2014_12