HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111632Generated: November 2, 2026
Diethyl chlorophosphate → HCID 44572352, compound
https://huagongshe.com/reaction/1111632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Ethyl isocyanoacetate | HCID 533707 | — |
| Reactant | Ro 7-9749 | HCID 3082318 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44572352 | HCID 44572352 | — |
Reaction Steps
A stirred solution of 3.8 g (0.01 mol) of 7-iodo-1,3-dihydro-5-(2-fluorophenyl)-2H-1,4-benzodiazepine-2-one in 50 ml of dimethyl formamide was cooled in an ice bath under an atmosphere of nitrogen. Potassium t-butoxide, 1.29 g (0.0115 mol) was added and after stirring for 5 minutes, 2.59 g (0.015 mol) of diethyl chlorophosphate was added and the stirring was continued for 5 minutes. A mixture of 2.26 g (0.02 mol) of ethyl isocyanoacetate in 50 ml of dimethylformamide that had been treated with 2.24 g (0.02 mol) of potassium t-butoxide just prior to the addition, was then added. After 5 minutes the ice bath was removed and the stirring was continued for 3 hours. The mixture was acidified with 2 ml of glacial acetic acid, diluted with 200 ml of saturated sodium bicarbonate solution and extracted with two 125 ml portions of toluene which were dried and evaporated. The residue was crystallized from ethyl acetate. For analysis, the crude product was chromatographed over silica gel using methylene chloride/ethyl acetate 1:1 (v/v) and then crystallized from ethyl acetate/hexane to give pure product with mp 200°-202°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04118386 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-af4f57c53ebf47a2ba77bbea8a9d81e1 |
|---|
| Source note | uspto-grants-1978_10 |
|---|