(S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

Base Information

Chemical Name:(S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester
CAS No.:108948-00-1
Molecular Formula:C₂₉H₃₇ClN₆O₅
Molecular Weight:585.103
Hs Code.:

Synonyms:(S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

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Chemical Property of (S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

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Technology Process of (S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

There total 4 articles about (S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester 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:

: 18144-47-3
tert-butyl 4-aminobenzoate

: 108948-00-1
(S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 45.7 percent / H₂ / Raney Ni / aq. acetic acid / Ambient temperature

2: 93 percent / CF₃COOH / CHCl₃ / 3 h / Ambient temperature

3: 1.) diethyl phosphorocyanidate, Et₃N / 1.) DMF, 65 deg C, 30 min, 2.) DMF, 65 deg C, 18 h

With diethyl cyanophosphonate; hydrogen; triethylamine; trifluoroacetic acid; nickel; In chloroform; acetic acid;
DOI:10.1021/jm00391a042

Reference yield:

: 18917-75-4
2,4-diamino-5-chloroquinazoline-6-carbonitrile

: 108948-00-1
(S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 45.7 percent / H₂ / Raney Ni / aq. acetic acid / Ambient temperature

2: 93 percent / CF₃COOH / CHCl₃ / 3 h / Ambient temperature

3: 1.) diethyl phosphorocyanidate, Et₃N / 1.) DMF, 65 deg C, 30 min, 2.) DMF, 65 deg C, 18 h

With diethyl cyanophosphonate; hydrogen; triethylamine; trifluoroacetic acid; nickel; In chloroform; acetic acid;
DOI:10.1021/jm00391a042

Reference yield:

: 108947-99-5
6-<(p-carboxyanilino)methyl>-5-chloro-2,4-diaminoquinazoline tert-butyl ester

: 108948-00-1
(S)-2-{4-[(2,4-Diamino-5-chloro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / CF₃COOH / CHCl₃ / 3 h / Ambient temperature

2: 1.) diethyl phosphorocyanidate, Et₃N / 1.) DMF, 65 deg C, 30 min, 2.) DMF, 65 deg C, 18 h

With diethyl cyanophosphonate; triethylamine; trifluoroacetic acid; In chloroform;
DOI:10.1021/jm00391a042