HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 86743635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-(Acetyloxy)-17-(butanoyloxy)-16-(1-methylpiperidin-1-ium-1-yl)-2-(piperidin-1-yl)androstane bromide | HCID 182554 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86743635 | HCID 86743635 | — |
Reaction Steps
Hydrogen chloride gas Was passed through a solution of 1-[(2β, 3α, 5α, 16β, 17α)-3-(acetyloxy)-17-(1-oxobutoxy)-2-(1-piperidinyl)-androstan-16-yl]-1-methylpiperidinium bromide, (0.5 g) in dichloromethane (40 ml), then the solution was evaporated to give a froth. The product was dissolved in acetone and diethyl ether was added to precipitate an amorphous solid, Which Was filtered off and washed with ether. The solid was heated under reflux in acetone to give 1-[(2β, 3α, 5α, 16β, 17α)-3-(acetyloxy)-17-(1-oxobutoxy)-2-(1-piperidinyl)-androstan-16-yl]-1-methylpiperidinium bromide hydrochloride as prisms (0.45 g), m.p. 220°-228° C., [α]D20 =+57.2° (c 1.32 in CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04891366 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-b9ff280bc862488c8f97a0fb453d4e12 |
| Source note | uspto-grants-1990_01 |