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2(1H)-Isoquinolinecarboxylic acid, 1-[(4-aminophenyl)methyl]-6,7-bis[(ethoxycarbonyl)oxy]-3,4-dihydro-, 9H-fluoren-9-ylmethyl ester

Base Information Edit
  • Chemical Name:2(1H)-Isoquinolinecarboxylic acid, 1-[(4-aminophenyl)methyl]-6,7-bis[(ethoxycarbonyl)oxy]-3,4-dihydro-, 9H-fluoren-9-ylmethyl ester
  • CAS No.:924651-73-0
  • Molecular Formula:C37H36N2O8
  • Molecular Weight:636.701
  • Hs Code.:
  • Mol file:924651-73-0.mol
2(1H)-Isoquinolinecarboxylic  acid,  1-[(4-aminophenyl)methyl]-6,7-bis[(ethoxycarbonyl)oxy]-3,4-dihydro-,  9H-fluoren-9-ylmethyl  ester

Synonyms:1-(4-amino-benzyl)-6,7-bis-ethoxycarbonyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid 9H-fluoren-9-ylmethyl ester

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Chemical Property of 2(1H)-Isoquinolinecarboxylic acid, 1-[(4-aminophenyl)methyl]-6,7-bis[(ethoxycarbonyl)oxy]-3,4-dihydro-, 9H-fluoren-9-ylmethyl ester Edit
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Technology Process of 2(1H)-Isoquinolinecarboxylic acid, 1-[(4-aminophenyl)methyl]-6,7-bis[(ethoxycarbonyl)oxy]-3,4-dihydro-, 9H-fluoren-9-ylmethyl ester

There total 5 articles about 2(1H)-Isoquinolinecarboxylic acid, 1-[(4-aminophenyl)methyl]-6,7-bis[(ethoxycarbonyl)oxy]-3,4-dihydro-, 9H-fluoren-9-ylmethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1: 95 percent / BBr3 / CH2Cl2 / cooling
2: 95 percent / pyridine / CH2Cl2 / 20 °C
3: 99 percent / H2 / Pd-C / ethyl acetate / 4 h / 3102.89 Torr
With pyridine; hydrogen; boron tribromide; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/j.bmc.2005.12.027
Guidance literature:
Multi-step reaction with 2 steps
1: 95 percent / pyridine / CH2Cl2 / 20 °C
2: 99 percent / H2 / Pd-C / ethyl acetate / 4 h / 3102.89 Torr
With pyridine; hydrogen; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/j.bmc.2005.12.027
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