HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → (2S, 4S, 5S)-5-(t-Butoxycarbonyl)amino-6-cyclohexyl-4-hydroxy-2-isopropyl-N-methylhexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | (3S, 5S)-5-[(1S)-1-(t-butoxycarbonyl)amino-2-cyclohexylethyl]-3-isopropyldihydrofuran-2(3H)-one | HCID 14217048 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2S, 4S, 5S)-5-(t-Butoxycarbonyl)amino-6-cyclohexyl-4-hydroxy-2-isopropyl-N-methylhexanamide | HCID 14483185 | 91% |
Reaction Steps
Gaseous methylamine was introduced into a solution of 1.33 g (3.76 mmole) of (3S, 5S)-5-[(1S)-1-(t-butoxycarbonyl)amino-2-cyclohexylethyl]-3-isopropyldihydrofuran-2(3H)-one (prepared as described in Preparation 1) in 10 ml of methanol to ensure saturation, whilst ice-cooling. The reaction vessel was then stoppered tightly and allowed to stand overnight. At the end of this time, the solvent was removed by distillation under reduced pressure and the residue was recrystallized from hexane to afford 1.32 g (yield 91%) of the title compound as white crystals, melting at 154°-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05378689 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-7c4b3b36fe814cd4af3a11878cc1d9fb |
| Source note | uspto-grants-1995_01 |