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tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate

Base Information Edit
  • Chemical Name:tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate
  • CAS No.:104436-88-6
  • Molecular Formula:C21H24N2O3
  • Molecular Weight:352.433
  • Hs Code.:
  • Mol file:104436-88-6.mol
tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate

Synonyms:tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate

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Chemical Property of tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate Edit
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Technology Process of tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate

There total 6 articles about tert-butyl 4-<(6-aminoindazol-1-yl)methyl>-3-methoxybenzoate 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:
With hydrogen; acetic acid; ethyl acetate; palladium on activated charcoal; for 24h; under 2585.7 Torr;
DOI:10.1021/jm00168a036
Guidance literature:
Multi-step reaction with 2 steps
1: 98 percent / K2CO3 / acetone / 48 h / Heating
2: 100 percent / acetic acid-EtOAc, H2 / 10percent Pd/C / 24 h / 2585.7 Torr
With hydrogen; potassium carbonate; acetic acid; ethyl acetate; palladium on activated charcoal; In acetone;
DOI:10.1021/jm00168a036
Guidance literature:
Multi-step reaction with 4 steps
1: 70 percent / conc. H2SO4 / CH2Cl2 / 16 h
2: 95 percent / N-bromosuccinimide, benzoyl peroxide / CCl4 / 1 h / Heating; Irradiation
3: 98 percent / K2CO3 / acetone / 48 h / Heating
4: 100 percent / acetic acid-EtOAc, H2 / 10percent Pd/C / 24 h / 2585.7 Torr
With N-Bromosuccinimide; Perbenzoic acid; sulfuric acid; hydrogen; potassium carbonate; acetic acid; ethyl acetate; palladium on activated charcoal; In tetrachloromethane; dichloromethane; acetone;
DOI:10.1021/jm00168a036
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