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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957621Generated: October 29, 2026

Methanimidamide, hydrochloride (1:1) → 6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepine

https://huagongshe.com/reaction/1957621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanimidamide, hydrochloride (1:1)HCID 10313058—
ReactantSodium MethoxideHCID 10942334—
Reactant4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-oneHCID 53653564—
SolventMethanolHCID 887—
Product6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepineHCID 54528139107.7%

Reaction Steps

To a solution of 0.152 g (1.89 mmol) of formamidine hydrochloride in 10 ml of methanol under argon is added 0.102 g (1.89 mmol) of sodium methoxide. After stirring 5 min., a solution of 0.46 g (1.26 mmol) of 4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepine-5-one in 5 ml of methanol is added and the mixture stirred 18 hours. The solvent is removed, dichloromethane added, and the mixture filtered. The solid is washed with dichloromethane. The combined filtrate is concentrated to dryness to give 0.47 g of tan foam. The preceding solid is purified by chromatography on silica gel. The compound is dissolved in ethyl acetate-dichloromethane and applied to the column. The column is then eluted with ethyl acetate to give 0.25 g of product as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05786353
Source datasetuspto-grants-1998_07
ORD IDord-d0b1f5a2d64941c8a6c40ed751b8fc71
Source noteuspto-grants-1998_07