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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763248Generated: October 31, 2026

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

https://huagongshe.com/reaction/1763248

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 numberUS04111931
Source datasetuspto-grants-1978_09
ORD IDord-3e8c5e8836d4410d84115c7bdb0376a4
Source noteuspto-grants-1978_09