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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464503Generated: October 29, 2026

Acetamidine monohydrochloride → HCID 13225499, compound

https://huagongshe.com/reaction/464503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 54487933HCID 54487933—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 13225499HCID 13225499—

Reaction Steps

A suspension of 5.1 g (0.015 mol) of 8-chloro-1-(2-fluorophenyl)-3,4-dihydro-4-[(dimethylamino)methylene]-5H-2-benzazepin-5-one and 2.1 g (0.0225 mol) of acetamidine hydrochloride in 150 ml of methanol was stirred at room temperature under argon, and treated with 2.4 g (0.045 mol) of sodium methylate in one portion. After stirring for 10 min, 90 ml of methylene chloride was added and stirring was continued. Another 2.4 g (0.045 mol) of sodium methylate and 2.1 g (0.0225 mol) of acetamidine hydrochloride were added after 2 hrs. The addition of 0.045 mol of sodium methylate and 0.0225 mol of acetamidine hydrochloride was repeated after another 2 hr interval and stirring at room temperature was continued overnight. After diluting with 150 ml of methylene chloride, the mixture was washed with water, dried over sodium sulfate and evaporated at reduced pressure. Recrystallization of the residue from hexane (charcoal) gave white crystals: mp 104°- 107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547581
Source datasetuspto-grants-1985_10
ORD IDord-396750d1b9464efbac4e3427c82372e0
Source noteuspto-grants-1985_10