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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254204Generated: October 26, 2026

Methylamine → (S)-tert-butyl 1-cyclohexyl-3-(methylamino)propan-2-ylcarbamate

https://huagongshe.com/reaction/1254204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(S)-2-(tert-butoxycarbonylamino)-3-cyclohexylpropyl methanesulfonateHCID 10735550—
SolventEthanolHCID 702—
Product(S)-tert-butyl 1-cyclohexyl-3-(methylamino)propan-2-ylcarbamateHCID 5938298047%

Reaction Conditions

Temperature55 °C

Reaction Steps

(S)-2-(tert-butoxycarbonylamino)-3-cyclohexylpropyl methanesulfonate (28 g, 83.6 mmol) was dissolved into a solution of methylamine in ethanol (about 30% by weight, 300 mL). The reaction was heated at 50-60° C. overnight and concentrated in vacuo. The residue was dissolved in EtOAc, washed with brine (2×100 mL), dried over MgSO4, and concentrated to give the crude product. This crude product was purified by flash chromatography (AcOEt:Hex.=2:1 first, then EtOAc: MeOH=1:1) to afford pure (S)-tert-butyl 1-cyclohexyl-3-(methylamino)propan-2-ylcarbamate (10.6 g, 47%). 1H NMR (400 MHz, CDCl3): 4.81 (brs, 1H), 3.89 (m, 1H), 2.77 (m, 2H), 2.54 (s, 3H), 2.44 (m, 2H), 1.78 (m, 1H), 1.67 (m, 4H), 1.44 (s, 9H), 1.50-1.10 (m, 6H), 1.00-0.77 (m, 2H), 0.05 (s, 9H). MS (E/Z): 271 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-1ebd700f6c9849cb85309261ae163c8d
Source noteuspto-grants-2013_06