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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644746Generated: October 30, 2026

tert-Butyl (2S)-2-methylpiperazine-1-carboxylate → 1,1-Dimethylethyl (2S)-2-methyl-4-{[6-(methylamino)-3-pyridinyl]methyl}-1-piperazinecarboxylate

https://huagongshe.com/reaction/644746

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
Reactant6-(Methylamino)nicotinaldehydeHCID 18416298—
Product1,1-Dimethylethyl (2S)-2-methyl-4-{[6-(methylamino)-3-pyridinyl]methyl}-1-piperazinecarboxylateHCID 59262209—

Reaction Steps

The title compound was prepared from 6-(methylamino)-3-pyridinecarbaldehyde (D95) and 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate using a method similar to that described for D81 in Description D81A. δH (CDCl3, 400 MHz) 7.97 (1H, d), 7.44 (1H, dd), 6.38 (1H, d), 4.51 (1H, m), 4.17 (1H, br.s), 3.79 (1H, d), 3.38 (1H, d), 3.26 (1H, d), 3.07 (1H, td), 2.92 (3H, d), 2.74 (1H, m), 2.57 (1H, m), 2.09 (1H, dd), 1.96 (1H, m), 1.45 (9H, s), 1.20 (3H, d). MS (ES+): 343.2 (MNa+), 265.2, no molecular ion (MH+) observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700599B2
Source datasetuspto-grants-2010_04
ORD IDord-c0b593a6501f4636b1e6908dc8be7218
Source noteuspto-grants-2010_04