HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → [(1-Chloro-4-methoxy-isoquinoline-3-carbonyl)-amino]-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | [(1-Chloro-4-methoxy-isoquinoline-3-carbonyl)-amino]-acetic acid methyl ester | HCID 86014583 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [(1-Chloro-4-methoxy-isoquinoline-3-carbonyl)-amino]-acetic acid | HCID 11737975 | — |
Reaction Steps
A mixture of [(1-chloro-4-methoxy-isoquinoline-3-carbonyl)-amino]-acetic acid methyl ester (21 mg, 0.07 mmol), KOH (23 mg, 0.35 mmol) and EtOH (1 ml) was stirred at ambient temperature for 3 h. Then the solvent was evaporated in vacuo. The residue was dissolved in water (2 ml) and the pH of the solution was adjusted to 2-3 by the addition of aqueous 1N HCl. The mixture was extracted with EtOAc (4×10 ml). The combined org. phases were dried over MgSO4 and evaporated in vacuo to give the title compound as a slightly yellowish solid (18 mg); MS-(+)-ion: M+1=295.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278325B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-a0c7b7bae4ba4ccf823c93b17c865657 |
| Source note | uspto-grants-2012_10 |