HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 2-isoquinolin-3-yl-1H-benzoimidazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2-Amino-3-[(isoquinoline-3-carbonyl)-amino]-benzoic acid methyl ester | HCID 66940314 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-isoquinolin-3-yl-1H-benzoimidazole-4-carboxylic acid | HCID 66940606 | 55% |
Reaction Steps
To a solution of the above crude product 2-amino-3-[(isoquinoline-3-carbonyl)-amino]-benzoic acid methyl ester in AcOH (25 mL) was added AcONH4 (16 g). The reaction mixture was refluxed for 3 h. After removal of AcOH under vacuum, the reaction mixture was washed with water (150 mL) The crude solid product 2-isoquinolin-3-yl-1H-benzoimidazole-4-carboxylic acid methyl ester was collected after filtration. LCMS: 304 (M+1)+. This product was hydrolyzed according to the general procedure C to provide 2-isoquinolin-3-yl-1H-benzoimidazole-4-carboxylic acid (1.6 g, 55% yield over three steps). LCMS: 290 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598353B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-7cebf4a27eed4dc4a297cc5b7b23211a |
| Source note | uspto-grants-2013_12 |