HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280868Generated: October 25, 2026
Hydrochloric Acid → Ethyl 3-{4-[4-({2-[17-(3-Carboxy-1-methylpropyl)-7,12-dihydroxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-3-yloxy]ethylcarbamoyl}methyl)phenoxy]-3,5-difluorophenyl}-2-methylacrylate
https://huagongshe.com/reaction/1280868
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-methyl-3-(3,4,5-trifluorophenyl)acrylate | HCID 53919072 | — |
| Reactant | HCID 69725368 | HCID 69725368 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-{4-[4-({2-[17-(3-Carboxy-1-methylpropyl)-7,12-dihydroxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-3-yloxy]ethylcarbamoyl}methyl)phenoxy]-3,5-difluorophenyl}-2-methylacrylate | HCID 69726546 | 62.4% |
Reaction Steps
610 mg of 4-(7,12-dihydroxy-3-{2-[2-(4-hydroxyphenyl)acetylamino]ethoxy}-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl)pentanoic acid, 232 mg of ethyl 2-methyl-3-(3,4,5-trifluorophenyl)acrylate and 393 mg of K2CO3 are suspended in 5 ml of DMF (anhydrous) and the suspension is stirred at 150° C. for 160 minutes. After cooling, the reaction mixture is taken up using 150 ml of a 2N aqueous HCl solution and extracted three times using 100 ml of EA each time. The extract is dried over Na2SO4 and the solvent is removed in vacuo. Chromatography on silica gel using EA/MeOH 10:1 yields 480 mg of resinous product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451781B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-d4b9aa4c49c34960b313b89001e25691 |
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| Source note | uspto-grants-2002_09 |
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