Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464580Generated: October 29, 2026

Formamidine acetate → HCID 13271775, compound

https://huagongshe.com/reaction/464580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
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 13271775HCID 13271775—

Reaction Steps

Dropwise 9.5 mL (41 mmol) of a 4.3M methanol solution of sodium methoxide was added to a solution of 8.0 g (22.6 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 6.5 g (62.4 mmol) of formamidine acetate in 70 mL of ethanol. When the addition was complete stirring at room temperature was continued for 30 min. The reaction was diluted with water and extracted with methylene chloride. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and concentrated at reduced pressure. The residue was crystallized from a mixture of ether and petroleum ether to give a yellow solid. Recrystallization from a mixture of ether and methylene chloride gave pale yellow prisms, mp 150°-155°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548750
Source datasetuspto-grants-1985_10
ORD IDord-140f7313b6ef42dc95034580338763a9
Source noteuspto-grants-1985_10