HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl isocyanate → HCID 12785879, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Hydroxylamine HCl | HCID 21645 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-dihydro-7-nitro-5-(o-chlorophenyl)-2H-1,4-benzodiazepine-2-thione | HCID 12371433 | — |
| Product | HCID 12785879 | HCID 12785879 | — |
Reaction Steps
2 g of 5-(2-chlorophenyl)-7-nitro-1,3-dihydro-2H-1,4-benzodiazepine-2-thione are reacted with 0.8 g of sodium bicarbonate and 0.7 g of hydroxylammonium chloride, analogously to Example 16. After stirring for 8 hours at room temperature, 0.8 ml of phenyl isocyanate are added, and the mixture is stirred for 1/2 an hour and precipitated with water; the oil produced is crystallized by means of ethanol. Recrystallization from ethanol yields 2 g of yellow crystals of melting point 201° to 203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395409 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-dd794fd9ec6e43c0b9ff3392f8554cb1 |
| Source note | uspto-grants-1983_07 |