HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (R)-3-[2-Cyclopropyl-7-(1,4-dimethyl-1H-indol-3-ylmethyl)-8-oxo-7,8-dihydro-purin-9-yl]-3-phenyl-propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | (R)-3-[2-Cyclopropyl-7-(1,4-dimethyl-1H-indol-3-ylmethyl)-8-oxo-7,8-dihydro-purin-9-yl]-3-phenyl-propionic acid ethyl ester | HCID 58497405 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-3-[2-Cyclopropyl-7-(1,4-dimethyl-1H-indol-3-ylmethyl)-8-oxo-7,8-dihydro-purin-9-yl]-3-phenyl-propionic acid | HCID 58497445 | 43% |
Reaction Steps
(R)-3-[2-Cyclopropyl-7-(1,4-dimethyl-1H-indol-3-ylmethyl)-8-oxo-7,8-dihydro-purin-9-yl]-3-phenyl-propionic acid ethyl ester (130 mg, 0.255 mmol) was dissolved in THF (3 ml). To the solution a concentrated solution of LiOH in water (2 ml) was added. The mixture was stirred at room temperature for 1 hour. The reaction was monitored by TLC. The reaction mixture was neutralized with 1N HCl, and then extracted with ethyl acetate 3×. The organic layer was dried over MgSO4, filtered and evaporated to dryness. The white solid obtained was purified by prep TLC, eluded with 10% methanol in dichloromethane to give the title compound (52 mg, 43%). LCMS, M++1, m/z: 481.54
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062056B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-45e623da7a7a49b199e699306022ec54 |
| Source note | uspto-grants-2015_06 |