HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451732Generated: October 26, 2026
Methylamine → (S)-tert-butyl 1-cyclohexyl-3-(methylamino)propan-2-ylcarbamate
https://huagongshe.com/reaction/451732
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | (S)-2-(tert-butoxycarbonylamino)-3-cyclohexylpropyl methanesulfonate | HCID 10735550 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-tert-butyl 1-cyclohexyl-3-(methylamino)propan-2-ylcarbamate | HCID 59382980 | 47% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487108B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-a2dd4f0552534a92bb1dc0a7a9f5ab84 |
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| Source note | uspto-grants-2013_07 |
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