HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 11620341, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | HCID 67304752 | HCID 67304752 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11620341 | HCID 11620341 | 72% |
Reaction Steps
16 mg (0.4 mmol) of sodium hydroxide are added to a solution of 70 mg (0.42 mmol) of methyl (S)-2-benzyloxy-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoate in 2 ml of 9/1 tetrahydrofuran/methanol. The reaction mixture is stirred overnight at ambient temperature. The reaction is halted by the addition of 2 ml of water and 0.5 ml of acetic acid, and then extraction is carried out with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated and then the residue is chromatographed on silica gel (dichloromethane/methanol 90/10). 49 mg of 2(S)-benzyloxy-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoic acid are obtained in the form of an oil. Yield=72%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07626054B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-db7e3c6458bc44098c77124d166c397a |
| Source note | uspto-grants-2009_12 |