HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Ammonia
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 57060556 | HCID 57060556 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 57019504 | HCID 57019504 | — |
Reaction Steps
The title compound was prepared by a similar method to Example 6 from (2S)-1-(1,3-benzoxazol-2-yl)-N2-(4-piperidinyl)-2-piperidinecarboxamide [see Example 31] and benzyl bromide. The crude product was purified by column chromatography on silica gel eluting with a solvent system of 93:7:1, by volume, dichloromethane:methanol: 0.88 aqueous ammonia solution to afford (2S)-1-(1,3-benzoxazol-2-yl)-N2-(1-benzyl-4-piperidinyl)-2-piperidinecarboxamide as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372736B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-397b9db84f1c4a0aab4598d92316001b |
| Source note | uspto-grants-2002_04 |