tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

Base Information

Chemical Name:tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate
CAS No.:943780-25-4
Molecular Formula:C₃₇H₃₉N₅O₃S
Molecular Weight:633.814
Hs Code.:

Synonyms:tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

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Chemical Property of tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

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Technology Process of tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

There total 7 articles about tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate 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: 68.0%

: 943780-24-3
4-chloro-7-isopropylquinazoline

: 943780-26-5
tert-butyl (S)-4-(2-amino-4-(1-phenylethylcarbamoyl)phenylthio)-phenylcarbamate

: 943780-25-4
tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

Guidance literature:: In ethanol; for 1h; Heating / reflux;

Reference yield:

: 586-61-8
4-iso-propylbromobenzene

: 943780-25-4
tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

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: trichlorophosphate / 1 h / Heating / reflux

7.1: ethanol / 1 h / Heating / reflux

With sulfuric acid; water; hydrogen; nitric acid; trichlorophosphate; palladium 10% on activated carbon; In methanol; ethanol; water; acetic acid; N,N-dimethyl-formamide;

Reference yield:

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

: 943780-25-4
tert-butyl (S)-4-(2-(7-isopropylquinazolin-4-ylamino)-4-(1-phenylethylcarbamoyl)phenylthio)phenylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

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

2: 0.5 h / 150 °C

3: trichlorophosphate / 1 h / Heating / reflux

4: ethanol / 1 h / Heating / reflux

With hydrogen; trichlorophosphate; palladium 10% on activated carbon; In methanol; ethanol;