HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20562330, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | 7-Aminoflunitrazepam | HCID 92294 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20562330 | HCID 20562330 | — |
Reaction Steps
4.2 g (0.015 M) of 7-amino-5-(o-fluorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one are heated at reflux for 3 hours in 80 ml of absolute tetrahydrofuran with 3.5 ml of chloroethylisocyanate and a catalytic amount of triethylamine. The mixture is left to stand at room temperature overnight. The solution is concentrated on a steam-bath and the residue is crystallised from ethyl acetate. There is obtained 1-(2-chloroethyl)-3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]urea which melts at 240° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04296031 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-fef24f57cbba4184b824cc82b38642b8 |
| Source note | uspto-grants-1981_10 |