HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 59539017, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | {4-[(Adamantan-1-ylmethyl)carbamoyl]pyrazolo[1,5-a]pyridin-2-ylmethoxy}acetic acid ethyl ester | HCID 25095104 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59539017 | HCID 59539017 | — |
Reaction Steps
3 M Aq. KOH (50 μL) is added to a solution of {4-[(adamantan-1-ylmethyl)carbamoyl]-pyrazolo[1,5-a]pyridin-2-ylmethoxy}acetic acid ethyl ester (11 mg, 25 μmol) and EtOH (250 μL). After 18 h, the volatiles are removed under reduced pressure. The residue is diluted with H2O (0.3 mL) and then acidified with 1 M aq. HCl. The title compound is collected by filtration. 1H NMR (400 MHz, ((CD3)2SO) δ: 8.74 (d, 1H), 8.42 (bs, 1H), 7.62 (d, 1H), 6.93 (t, 1H), 6.84 (s, 1H), 4.70 (s, 2H), 4.08 (s, 2H), 2.99 (d, 2H), 1.86-2.00 (m, 3H), 1.48-1.73 (m, 12H). LC-MS m/z (M+H+): 398.3; RT=1.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580812B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-dbcef0cbb8984d3d82956851d434eac4 |
| Source note | uspto-grants-2013_11 |