HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepin-10-yl)-2-oxoethyl]-3-(ethylthio)propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 10-(Aminoacetyl)-8-chloro-10,11-dihydrodibenz-[b,f][1,4]oxazepine | HCID 10661061 | — |
| Reactant | 3-(Ethylsulfanyl)propanoyl chloride | HCID 12850617 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-(8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepin-10-yl)-2-oxoethyl]-3-(ethylthio)propanamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212169 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-09b404f8fcde47f7a35e5411322b5f67 |
| Source note | uspto-grants-1993_05 |