HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288046Generated: October 31, 2026
Phosphorus sulfide (P2S5) → HCID 20360389, compound
https://huagongshe.com/reaction/1288046
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | 1,4-BENZDIAZEPIN-2-ONE-5(26F-PH)7CL | HCID 23275763 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20360389 | HCID 20360389 | — |
Reaction Steps
A solution of 7.65 g. (0.025 mole) of 1,3-dihydro-7-chloro-5-(2,6-difluorophenyl)-2H-1,4-benzodiazepin-2-one in 500 ml. of pyridine was treated with 5.55 g. (0.025 mole) of phosphorus pentasulfide and heated under reflux in a nitrogen atmosphere for two hours. The pyridine (350 ml.) was removed in vacuo and the thus-produced residue was poured onto crushed ice. The aqueous phase was extracted with methylene chloride and then discarded. The extract was washed successively with three 200-ml. portions of water and 100 ml. of brine, and dried over anhydrous sodium sulfate. Removal of the solvent gave 7.0 g. of solid which was recrystallized from ethanol-water, to give in 2 crops 6.8 g. of crude material which, after recrystallization from ethanol-water, gave pure 1,3-dihydro-7-chloro-5-(2,6-difluorophenyl)-2H-1,4-benzodiazepine-2-thione of melting point 222.5°-224° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03987052 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-6a704f258c974d1ba016075fd15db545 |
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| Source note | uspto-grants-1976_10 |
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