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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295973Generated: October 30, 2026

Acetamidine monohydrochloride → HCID 13271777, compound

https://huagongshe.com/reaction/2295973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantSodium MethoxideHCID 10942334—
ReactantButyl 8-chloro-1-phenyl-3H-2-benzazepine-5-carboxylateHCID 13271771—
ReactantButyl 8-chloro-1-phenyl-5H-2-benzazepine-5-carboxylateHCID 13271773—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 13271777HCID 13271777—

Reaction Steps

In one portion, 11.5 mL (49 mmol) of a 4.34 M methanol solution of sodium methoxide was added to a solution of 11.0 g (31 mmol) of a mixture of 8-chloro-1-phenyl-5H-2-benzazepine-5-carboxylic acid butyl ester and 8-chloro-1-phenyl-3H-2-benzazepine-5-carboxylic acid butyl ester and 5.7 g (60 mmol) of acetamidine hydrochloride in 200 mL of ethanol. The mixture was refluxed for 18 hr, cooled and poured into 800 mL of water. The resulting precipitate was collected by filtration and washed with ether to yield a yellow solid. Recrystallization from tetrahydrofuran gave off-white prisms, mp 155°-160°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427589
Source datasetuspto-grants-1984_01
ORD IDord-c7125d6ff43d4451a86e2ebff6065e63
Source noteuspto-grants-1984_01