HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 23000834, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl [(3E)-4-(acetylsulfanyl)-3-(2-ethoxy-2-oxoethylidene)piperidin-1-yl](2-chlorophenyl)acetate | HCID 15462957 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23000834 | HCID 23000834 | — |
Reaction Steps
1.22 g of the (E)-4-acetylthio-1-(2-chloro-α-methoxycarbonylbenzyl)-3-ethoxycarbonylmethylidenepiperidine obtained in the above-described step (a) were dissolved in 50 ml of methanol was dissolved. An appropriate amount of hydrogen chloride gas was blown through the resulting solution and the resulting mixture was allowed to stand overnight at room temperature. The residue after the removal of the solvent under reduced pressure was crystallized from diethyl ether, whereby 1.25 g of a mixture of (E)-1-(2-chloro-α-methoxycarbonylbenzyl)-3-ethoxycrbonylmethylidene-4-mercaptopiperidine hydrochloride and (E)-1-(2-chloro-α-methoxycarbonylbenzyl)-4-mercapto-3-methoxycarbonylmethylidene-piperidine hydrochloride was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610708B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-250f6f24d07e486fb2dc61bee20a22a5 |
| Source note | uspto-grants-2003_08 |