4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

Base Information

Chemical Name:4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid
CAS No.:943780-29-8
Molecular Formula:C₂₉H₃₀N₄O₄S
Molecular Weight:530.648
Hs Code.:

Synonyms:4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

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Chemical Property of 4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

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Technology Process of 4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

There total 10 articles about 4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid 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: 88.0%

: 943780-28-7
methyl 4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoate

: 943780-29-8
4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

Guidance literature:: methyl 4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoate; With lithium hydroxide; In 1,4-dioxane; water; at 20 - 50 ℃; for 1h;

With hydrogenchloride; In 1,4-dioxane; water; pH=1;

Reference yield:

: 35480-95-6
4-isopropyl-2-nitro-benzoic acid

: 943780-29-8
4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 760.05 Torr

2.1: 0.5 h / 150 °C

3.1: ethanol / 0.5 h / Heating / reflux

4.1: lithium hydroxide / 1,4-dioxane; water / 1 h / 20 - 50 °C

4.2: pH 1

With lithium hydroxide; hydrogen; palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethanol; water;

Reference yield:

: 586-61-8
4-iso-propylbromobenzene

: 943780-29-8
4-(4-(tert-butoxycarbonylamino)phenylthio)-3-(7-isopropylquinazolin-4-ylamino)benzoic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: nitric acid / water / 2 h / 5 - 10 °C

2.1: N,N-dimethyl-formamide / 1.5 h / 160 °C

2.2: 0.33 h / 65 °C

3.1: sulfuric acid; water / acetic acid / 72 h / Heating / reflux

3.2: 0 °C / pH 12

3.3: pH 2

4.1: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 760.05 Torr

5.1: 0.5 h / 150 °C

6.1: ethanol / 0.5 h / Heating / reflux

7.1: lithium hydroxide / 1,4-dioxane; water / 1 h / 20 - 50 °C

7.2: pH 1

With lithium hydroxide; sulfuric acid; water; hydrogen; nitric acid; palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethanol; water; acetic acid; N,N-dimethyl-formamide;