HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 5-Chloro-7,8-dimethoxy-1-methyl-1,3-dihydro-1,4-benzodiazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7,8-dimethoxy-1-methyl-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione | HCID 69155597 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-Chloro-7,8-dimethoxy-1-methyl-1,3-dihydro-1,4-benzodiazepin-2-one | HCID 69154852 | — |
Reaction Steps
Heat at 125° C. in a sealed tube for 3Y4 hour a solution of 100 mg (0.40 mmol) of 7,8-dimethoxy-1-methyl-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione (XVIIaa), 280 μl of dimethylaniline, 800 μl of POCl3, in 10 ml of anhydrous CHCl3. Allow to cool to room temperature. Add 3 g of silica and 5 ml of CH2Cl2. Add at 0° C., 1 ml of triethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250410B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-70924f78099548cd8820a2a050bcdd2a |
| Source note | uspto-grants-2007_07 |