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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293202Generated: October 30, 2026

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

https://huagongshe.com/reaction/2293202

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 numberUS05686445
Source datasetuspto-grants-1997_11
ORD IDord-d7f4f69de2214bbaa9fc66abecaa17a9
Source noteuspto-grants-1997_11