HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Alanine → (S)-2-{[1-bromo-4-hydroxy-isoquinoline-3-carbonyl]-amino}-propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester | HCID 86014541 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-2-{[1-bromo-4-hydroxy-isoquinoline-3-carbonyl]-amino}-propionic acid | HCID 86595466 | — |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
400 mg of 1-bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester and 890 mg of (L)-Alanine was suspended in a 20 ml solution of 0.5 M of sodium methoxide in methanol. The mixture was heated to 160° C. for 12 min using a CEM Discover microwave reactor. The resultant solution was concentrated to ca. 10 ml, and 0.5 N HCl was added until a pH 3 was reached. The solution was extracted three times with ethyl acetate, and the organic fractions dried over sodium sulfate and concentrated to a tan solid; MS (−): m/z 337.14 (M−1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765956B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-e6c52e935f3d42638da6c164131641ca |
| Source note | uspto-grants-2014_07 |