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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248823Generated: November 1, 2026

Triethylamine → N-[2-(8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepin-10-yl)-2-oxoethyl]-3-(ethylthio)propanamide

https://huagongshe.com/reaction/248823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant10-(Aminoacetyl)-8-chloro-10,11-dihydrodibenz-[b,f][1,4]oxazepineHCID 10661061—
Reactant3-(Ethylsulfanyl)propanoyl chlorideHCID 12850617—
SolventDichloromethaneHCID 6344—
ProductN-[2-(8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepin-10-yl)-2-oxoethyl]-3-(ethylthio)propanamideHCID 10692640—

Reaction Steps

A solution of 3-(ethylthio)propanoyl chloride (0.87 grams) in methylene chloride (10 mL) was added dropwise to a stirred solution of 10-(aminoacetyl)-8- chloro-10,11-dihydrodibenz-[b,f][1,4]oxazepine (1.50 grams) and triethylamine (0.84 mL) in methylene chloride (40 mL) in an ice bath at 5° C. under nitrogen. The ice bath was removed, and the reaction was stirred for 3 hours. The reaction was diluted with methylene chloride (50 mL) and washed with 50 mL each of 1N HCl, saturated aqueous sodium bicarbonate, and brine. The solution was then dried over MgSO4 and evaporated in vacuo. The yield of the title compound was 1.90 grams (90%). Mp: 148°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212169
Source datasetuspto-grants-1993_05
ORD IDord-09b404f8fcde47f7a35e5411322b5f67
Source noteuspto-grants-1993_05