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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732205Generated: October 30, 2026

Aminoacetaldehyde dimethyl acetal → HCID 178495895, compound

https://huagongshe.com/reaction/1732205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant3H-1,3,4-Benzotriazepine, 7-chloro-3-methyl-2-(methylthio)-5-phenyl-HCID 628794—
SolventGlycol monoethyl etherHCID 8076—
ProductHCID 178495895HCID 178495895—

Reaction Steps

A mixture of 2.66 grams (8.42 m moles) o=7-chloro-3-methyl-2-(methylthio)-5-phenyl-3H-1,3,4-benzotriazepine, 1.0 grams (9.32 m moles) of aminoacetaldehyde dimethyl acetal (98%) and 10 ml of 2-ethoxyethanol was stirred and refluxed under nitrogen for about 18 hours. The solvent was removed in vacuo on a rotary evaporator, and the residue was dissolved in diethyl ether. The resulting solution was washed in water, dried with magnesium sulfate and concentrated in vacuo. The dark residue was found to be a mixture and was chromatographed on a column containing 170 grams of alumina. The column was washed with benzene. The desired dimethoxyethylamino-1,3,4-benzotriazepine intermediate was obtained on elution with successive portions of methylene chloride and chloroform. The fractions were combined and evaporated to yield a red viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237049
Source datasetuspto-grants-1980_12
ORD IDord-367bbbd661174cffaaeb439c7fd278cd
Source noteuspto-grants-1980_12