HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 10164916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18449085 | HCID 18449085 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10164916 | HCID 10164916 | — |
Reaction Steps
The crude 10-(4-cyclohexyl-benzoyl)-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-carbonyl chloride prepared in the manner of Example 23 (1.0 g) was added to a stirred mixture of N,N-diisopropylethyl amine (0.31 g) and 4-methoxy aniline (0.35 g) in dichloromethane (25 mL). After stirring overnight at room temperature the reaction mixture was washed with water and saturated aqueous sodium bicarbonate, and dried over anhydrous sodium sulfate. The solution was filtered through a short column of Magnesol® and the eluate evaporated to dryness to provide the desired title compound (1.0 g) as an off-white amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202239B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-c116538f044f4c55912722d863d69f08 |
| Source note | uspto-grants-2007_04 |