HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-{3-[2-(3-Bromobenzoylamino)ethoxy]-7,12-dihydroxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl}pentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-{3-[2-(3-bromobenzoylamino)ethoxy]-7,12-dihydroxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl}pentanoate | HCID 18425126 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-{3-[2-(3-Bromobenzoylamino)ethoxy]-7,12-dihydroxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl}pentanoic acid | HCID 18425128 | 93.7% |
Reaction Steps
600 mg of methyl 4-{3-[2-(3-bromobenzoylamino)ethoxy]-7,12-dihydroxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl}pentanoate are dissolved in 19 ml of methanol and 4.6 ml of a 1N aqueous NaOH solution are added. The mixture is stirred at RT for 6 hours, then poured into 150 ml of a 2N aqueous HCl solution and extracted 4 times using 150 ml of MTB each time. The extract is dried over Na2SO4 and the solvent is removed in vacuo. 550 mg of a viscous oil are obtained, which are employed further as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451781B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-71eec1ada0954e84834435dd77eb2580 |
| Source note | uspto-grants-2002_09 |