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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614710Generated: October 30, 2026

Dimethylformamide → 7-Chloro-5-phenyl-1,2,3,4-tetrahydro-2-nitromethylene-5H-1, 5-benzodiazepin-4-one

https://huagongshe.com/reaction/614710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantNitromethaneHCID 6375—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant8-chloro-4-(nitrosomethylamino)-1-phenyl-3H-1,5-benzodiazepin-2-oneHCID 178526374—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product7-Chloro-5-phenyl-1,2,3,4-tetrahydro-2-nitromethylene-5H-1, 5-benzodiazepin-4-oneHCID 70605628—

Reaction Steps

Potassium t-butoxide, 10.24 g (0.092 moles) was added to a mixture of 250 ml of dimethylformamide and 50 ml of nitromethane. After stirring at room temperature for 15 min under nigrogen, 25 g (0.076 m) of 7-chloro-3,5-dihydro-2-(N-nitrosomethylamino)-5-phenyl-4H-1,5-benzodiazepin-4-one was added and stirring was continued for an additional 19 hours. The mixture was acidified with acetic acid and diluted with water. The precipitate was filtered off, washed with water and recrystallized from methylene chloride/ethanol to give pale yellow crystals with mp 259°-261°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04146537
Source datasetuspto-grants-1979_03
ORD IDord-c27583d2e35e49f7953ec262755c4d74
Source noteuspto-grants-1979_03