HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844975Generated: October 30, 2026
O-Phenylenediamine → HCID 178507510, compound
https://huagongshe.com/reaction/1844975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 58026665 | HCID 58026665 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178507510 | HCID 178507510 | 80% |
Reaction Steps
To a solution of 0.33 g (1.0 mmol) of -[(isoquinoline-1-carbonyl)-amino]-3H-benzoimidazole-4-carboxylic acid (from Example 58) in DMF (5 mL) was added 0.47 g (1.25 mmol) of HBTU and DIEA (0.5 mL). The mixture was stirred for 5 min, then 0.22 g (2.0 mmol) of benzene-1,2-diamine was added in one portion. The reaction mixture was heated at 50° C. for 1 h, after cooling to room temperature, the coupling product was precipitated by addition of sat. aq. sodium carbonate solution (15 mL). The solid was filtered, washed with water, and dried to provide 0.35 g (80%) of isoquinoline-1-carboxylic acid [7-(2-amino-phenylcarbamoyl)-1H-benzoimidazol-2-yl]-amide. LCMS: 443 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946259B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-703d2dbfd8b844929de759c1924d4d6f |
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| Source note | uspto-grants-2015_02 |
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