HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivalaldehyde → HCID 67025694, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | HCID 67025677 | HCID 67025677 | — |
| Product | HCID 67025694 | HCID 67025694 | — |
Reaction Steps
In analogy to the procedure described for the synthesis of example 104, the title compound N-{(3RS,4SR)-4-(4-chloro-phenyl)-1-[1-(2,2-dimethyl-propyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-methoxy-N-methyl-3-trifluoromethyl-benzamide was prepared from N-[(3RS,4SR)-4-(4-chloro-phenyl)-1-(piperidine-4-carbonyl)-pyrrolidin-3-yl]-4-methoxy-N-methyl-3-trifluoromethyl-benzamide using trimethylacetaldehyde (75% in tert butanol) instead of acetone and was obtained as a light brown oil. MS m/e: 594.3 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08404679B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-109b0d90afb542b3a4f84c958a135242 |
| Source note | uspto-grants-2013_03 |