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

Base Information

Chemical Name:tert-butyl 5-(2-(3-(oxazol-2-ylmethoxy)phenyl)-quinazolin-4-ylamino)-1H-indazole-1-carboxylate
CAS No.:1024582-75-9
Molecular Formula:C₃₀H₂₆N₆O₄
Molecular Weight:534.574
Hs Code.:

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

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

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

There total 8 articles about tert-butyl 5-(2-(3-(oxazol-2-ylmethoxy)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:

: 28144-70-9,88-68-6
anthranilic acid amide

: 1024582-75-9
tert-butyl 5-(2-(3-(oxazol-2-ylmethoxy)phenyl)-quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1.1: pyridine / chloroform / 6 h / 20 °C

2.1: sodium hydroxide / water / 4 h / Heating / reflux

2.2: 2 h / 20 °C / pH 7

3.1: boron tribromide / dichloromethane / 4 h / -78 - 20 °C

3.2: 0.5 h / -78 - 20 °C

3.3: pH 7

4.1: pyridine / 3.5 h / 105 °C

5.1: thionyl chloride; N,N-dimethyl-formamide / 4 h / Heating / reflux

6.1: isopropyl alcohol / 0.5 h / 95 °C

7.1: methanol; ammonia; water / 48 h / 20 °C

8.1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 1 h / 70 °C

With pyridine; methanol; sodium hydroxide; thionyl chloride; ammonia; water; boron tribromide; potassium carbonate; N,N-dimethyl-formamide; potassium iodide; In dichloromethane; chloroform; water; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 185246-17-7
2-(chloromethyl)oxazole

: 911417-26-0
tert-butyl 5-(2-(3-hydroxyphenyl)-quinazolin-4-ylamino)-1H-indazole-1-carboxylate

: 1024582-75-9
tert-butyl 5-(2-(3-(oxazol-2-ylmethoxy)phenyl)-quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Guidance literature:: With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 70 ℃; for 1h;

Reference yield:

: 911417-23-7
2-(3-hydroxylphenyl)quinazolin-4(3H)-one

: 1024582-75-9
tert-butyl 5-(2-(3-(oxazol-2-ylmethoxy)phenyl)-quinazolin-4-ylamino)-1H-indazole-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / 3.5 h / 105 °C

2: thionyl chloride; N,N-dimethyl-formamide / 4 h / Heating / reflux

3: isopropyl alcohol / 0.5 h / 95 °C

4: methanol; ammonia; water / 48 h / 20 °C

5: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 1 h / 70 °C

With pyridine; methanol; thionyl chloride; ammonia; water; potassium carbonate; N,N-dimethyl-formamide; potassium iodide; In N,N-dimethyl-formamide; isopropyl alcohol;