Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613133Generated: November 1, 2026

Methylamine → HCID 14986581, compound

https://huagongshe.com/reaction/1613133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 14986580HCID 14986580—
SolventEthanolHCID 702—
ProductHCID 14986581HCID 14986581—

Reaction Conditions

Temperature4 °C

Reaction Steps

3-Carbethoxyamino-5-(α-bromopropionyl)-5H-dibenz[b,f]-azepine (10 g) is mixed with 15 ml of approximately 35% aqueous methylamine solution and 75 ml of ethanol and heated in a laboratory autoclave for 12 hours at 90° to 95° C. After cooling to 4° C., the formed precipitate is filtered off with suction, mixed with 50 ml of acetone and then, again filtered off with suction and dried. 3-Carbethoxyamino-5-(α-methylaminopropionyl)-5H-dibenz[b,f]azepine (7 g) is obtained, which can be purified by being dissolved in dilute hydrochloric acid and precipitated with concentrated ammonia solution. The purified compounds melts at 217° to 219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192760
Source datasetuspto-grants-1993_03
ORD IDord-c2cbe3ade56d440dafa9ff7164e7e5bb
Source noteuspto-grants-1993_03