HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509087Generated: October 31, 2026
O-Phenylenediamine → HCID 86731465, compound
https://huagongshe.com/reaction/509087
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | HCID 86731464 | HCID 86731464 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86731465 | HCID 86731465 | 109.4% |
Reaction Steps
To a solution of 7-(4-(tert-butoxycarbonyl)piperazin-1-yl)-8-cyclopropylisoquinoline-3-carboxylic acid (60 mg, 0.15 mmol) and o-Phenylenediamine (16 mg, 0.15 mmol) in DMF (5 mL) was added HOAT (41 mg, 0.3 mmol), EDCI (46 mg, 0.3 mmol), and DIPEA (77 mg, 0.6 mmol). The reaction mixture was stirred at 60° C. overnight. After extraction by EA, the combined organic layers were dried by anhydrous Na2SO4 and concentrated in vacuo to afford tert-butyl 4-(3-(2-aminophenylcarbamoyl)-8-cyclopropylisoquinolin-7-yl)piperazine-1-carboxylate as a yellow solid (80 mg, yield: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096549B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-a03f442d587d4666a345a6742b3bc719 |
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| Source note | uspto-grants-2015_08 |
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