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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534776Generated: October 29, 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/534776

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 numberUS08853218B2
Source datasetuspto-grants-2014_10
ORD IDord-a883e115a4e94963a7e7a262c214d925
Source noteuspto-grants-2014_10