HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 58312634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | 4-Fluorophenyl chloroformate | HCID 2733256 | — |
| Reactant | HCID 58312647 | HCID 58312647 | — |
| Product | HCID 58312634 | HCID 58312634 | — |
Reaction Steps
In analogy to the procedure described for the synthesis of rac-{(3S,4R)-4-(3,4-Dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-ethyl-carbamic acid 4-fluoro-phenyl ester (example 1, step g & h) the title compound was prepared from (3S,4R)-1-Benzyl-4-(4-chloro-3-fluoro-phenyl)-pyrrolidin-3-ylamine through reductive amination with acetaldehyde followed by reaction with 4-fluorophenyl chloroformate to yield the title compound as light brown oil. MS m/e: 471.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346786B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-e74a0ab0330a4c0ab9dd58fbfa8fc680 |
| Source note | uspto-grants-2016_05 |