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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076200Generated: October 31, 2026

Phosphorus sulfide (P2S5) → HCID 24104717, compound

https://huagongshe.com/reaction/1076200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus sulfide (P2S5)HCID 14817—
Reactant7-chloro-5H-dibenzo[b,e][1,4]diazepin-11(10H)-oneHCID 21539232—
SolventPyridineHCID 1049—
ProductHCID 24104717HCID 24104717—

Reaction Steps

A mixture of 7-chloro-5,10-dihydro-11H-dibenzo[b,e]-[1,4]diazepin-11-one (30.5 g., 0.125 mole), phosphorus pentasulfide (27.8 g., 0.131 mole) and one l. of pyridine is heated at reflux temperature for 4 hours and the pyridine is evaporated in vacuo. The residue is stirred for 1 hour with one l. each of saturated aqueous sodium bicarbonate and methylene chloride and filtered to remove some solid product. The organic layer of the filtrate is washed successively with sodium bicarbonate solution and with saturated salt solution, dried over anhydrous magnesium sulfate and evaporated. The residue is combined with the solid obtained above and triturated with hot chloroform and methanol. In this way, 12.2 g. of 7-chloro-5,10-dihydro-11H-dibenzo[b,e][1,4]diazepine-11-thione of melting point 274°-275° C is obtained. Concentration of the chloroform-methanol washings affords an additional 8.4 g. of product having the same melting point. Recrystallization from dimethylformamide-water gives an analytically pure sample in the form of pale yellow needles of melting point 276°-277° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956297
Source datasetuspto-grants-1976_05
ORD IDord-9fa84ab32dff40238aeac1361602e05b
Source noteuspto-grants-1976_05