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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509087Generated: October 31, 2026

O-Phenylenediamine → HCID 86731465, compound

https://huagongshe.com/reaction/509087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantHCID 86731464HCID 86731464—
SolventDimethylformamideHCID 6228—
ProductHCID 86731465HCID 86731465109.4%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096549B2
Source datasetuspto-grants-2015_08
ORD IDord-a03f442d587d4666a345a6742b3bc719
Source noteuspto-grants-2015_08