HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 70455044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2-Chloroethyl)-N-methylbenzylamine hydrochloride | HCID 12822620 | — |
| Reactant | (+)-cis-2-(4-methoxyphenyl)-3-acetoxy-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one | HCID 70453288 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 70455044 | HCID 70455044 | 69.6% |
Reaction Steps
A mixture of 3.0 g of (-)-cis-2-(4-methoxyphenyl)-3-acetoxy-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, 1.9 g of 2-(N-benzyl-N-methylamino)ethyl chloride.hydrochloride, 3.3 g of potassium carbonate and 80 ml of acetone is refluxed for 20 hours. Insoluble materials are removed by filtration, and the filtrate is evaporated under reduced pressure to remove solvent. The residue is dissolved in ethyl acetate, and the solution is washed with water, dried and evaporated to remove solvent. 2.9 g of (-)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(N-benzyl-N-methylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one are obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04585768 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-bb574e6331414e3a91b3cddf1199dc33 |
| Source note | uspto-grants-1986_04 |