HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-1-Boc-4-aminomethyl-3-hydroxypiperidine → HCID 11015727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | trans-1-Boc-4-aminomethyl-3-hydroxypiperidine | HCID 11075229 | — |
| Reactant | HCID 88040818 | HCID 88040818 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11015727 | HCID 11015727 | 80% |
Reaction Steps
A mixture of intermediate (1-e) (0.087 mol) and intermediate (3-a) (0.087 mol) in acetonitrile (600 ml) was stirred and refluxed for 90 min. The reaction mixture was cooled, and the solvent was evaporated. The residue was partitioned between DCM and water. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was suspended in DIPE with a drop of ACN, filtered off and dried (vacuum, 40° C.), yielding 30.3 g (80%) of (±)-1,1-dimethylethyl trans-4-[[(4-amino-5-chloro-2,3-dimethoxybenzoyl)amino]methyl]-3-hydroxy-1-piperidinecarboxylate (interm. 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06750349B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-f649c2ede5634f988e45339bcfac2953 |
| Source note | uspto-grants-2004_06 |