HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → 5-(5-Chloro-2-methoxy-4-methyl-phenyl)-1-(2-cyclopropyl-ethyl)-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 2-Bromo-1-(5-chloro-2-methoxy-4-methylphenyl)ethanone | HCID 2756888 | — |
| Reactant | Cyclopropaneethanamine | HCID 10240761 | — |
| Product | 5-(5-Chloro-2-methoxy-4-methyl-phenyl)-1-(2-cyclopropyl-ethyl)-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamide | HCID 58999098 | — |
Reaction Steps
The title compound was synthesized in analogy to Example 68, using 3-oxo-butyric acid methyl ester as compound of formula R, 2-bromo-1-(5-chloro-2-methoxy-4-methyl-phenyl)-ethanone as compound of formula S, 2-cyclopropyl-ethylamine as R3—(CH2)m—NH2 and cyclohexylamine as R1R2NH, MS (ISP) 429.6 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579369B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-d6abc013c10a42748a3e4e12febc2e3c |
| Source note | uspto-grants-2009_08 |