Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 66660665 | HCID 66660665 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 49838811 | HCID 49838811 | — |
Reaction Steps
1-[4′-(4-{1-[3-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-ethoxycarbonylamino}-3-methyl-isoxazol-5-yl)-biphenyl-4-yl]-cyclopropanecarboxylic acid ethyl ester (0.400 g, 0.63 mmol) in 3:1 MeOH:H2O (10 mL) was treated with excess lithium hydroxide. The reaction was stirred overnight at 60° C., and then acidified and extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated, and the residue was purified by preparative HPLC to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273780B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-aa35d170b7664518ba1d0f12fd92c1fd |
|---|
| Source note | uspto-grants-2012_09 |
|---|