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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184644Generated: October 31, 2026

Formaldehyde → HCID 66733152, compound

https://huagongshe.com/reaction/1184644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydride [MI]HCID 20587905—
ReactantHCID 66732904HCID 66732904—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 66733152HCID 66733152116.9%

Reaction Steps

1-{7-Chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonylmethyl}-piperazine dihydrochloride (400 mg, 0.62 mmol), formalin (0.15 ml, 1.9 mmol), sodium acetate (61 mg, 0.74 mmol), and sodium cyanotrihydroborate (119 mg, 1.9 mmol) were added to methanol (5 ml), and the mixture was stirred at room temperature for 1 hour. Water and aqueous sodium hydroxide solution were added to the reaction mixture, and the precipitates were collected by filtration, washed with water, and then dried. The obtained solid was dissolved in ethyl acetate, and a 4N hydrogen chloride ethyl acetate solution (0.5 ml) was added thereto. The precipitates were then collected by filtration, washed with ethyl acetate and dried to obtain 240 mg of 1-{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonylmethyl}-4-methyl-piperazine dihydrochloride as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669229B2
Source datasetuspto-grants-2014_03
ORD IDord-184f3e609be14554b541b03e16c84ea4
Source noteuspto-grants-2014_03