HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → 5-(5-Chloro-2-methoxy-4-methyl-phenyl)-1-cyclopropylmethyl-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | 2-Bromo-1-(5-chloro-2-methoxy-4-methylphenyl)ethanone | HCID 2756888 | — |
| Product | 5-(5-Chloro-2-methoxy-4-methyl-phenyl)-1-cyclopropylmethyl-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamide | HCID 58999097 | — |
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, cyclopropanemethylamine as R3—(CH2)m—NH2 and cyclohexylamine as R1R2NH, MS (ISP) 415.5 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07294644B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-6a3bd44da30d4e7c97074eaffcb618c5 |
| Source note | uspto-grants-2007_11 |