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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021869Generated: October 30, 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/1021869

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 8668373093.1%

Reaction Steps

Following the procedure described for compound 101h and starting with (3S)-tert-butyl 3-methyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylate 191e (5.8 g, 18 mmol) afforded 191f as a brown solid (4.9 g, 93%). MS-ESI: [M+H]+ 293

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716274B2
Source datasetuspto-grants-2014_05
ORD IDord-71f2a394d1ab4d25acc1cef045888518
Source noteuspto-grants-2014_05