tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Base Information

Chemical Name:tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate
CAS No.:911417-47-5
Molecular Formula:C₂₈H₂₅ClN₆O₃
Molecular Weight:528.998
Hs Code.:

Synonyms:tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

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Chemical Property of tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

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Technology Process of tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

There total 7 articles about tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate 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:

Reference yield: 87.0%

: 911417-28-2
tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

: 79-04-9
chloroacetyl chloride

: 911417-47-5
tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; water; ethyl acetate; at 20 ℃; for 6h;

Reference yield:

: 911417-27-1
tert-butyl 5-(2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

: 911417-47-5
tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / methanol; 1,2-dimethoxyethane / 16 h / 20 °C

2: sodium hydrogencarbonate / tetrahydrofuran; water; ethyl acetate / 6 h / 20 °C

With hydrogen; sodium hydrogencarbonate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; water; ethyl acetate;

Reference yield:

: 34637-85-9
2-(3-nitrophenyl)-(3H)-4-quinazolinone

: 911417-47-5
tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride; N,N-dimethyl-formamide / 4.5 h / Heating / reflux

2: isopropyl alcohol / 1.5 h / 95 °C

3: hydrogen / palladium 10% on activated carbon / methanol; 1,2-dimethoxyethane / 16 h / 20 °C

4: sodium hydrogencarbonate / tetrahydrofuran; water; ethyl acetate / 6 h / 20 °C

With thionyl chloride; hydrogen; sodium hydrogencarbonate; N,N-dimethyl-formamide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; water; ethyl acetate; isopropyl alcohol;