(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

Base Information

Chemical Name:(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester
CAS No.:161878-87-1
Molecular Formula:C₃₅H₄₇N₅O₇
Molecular Weight:649.787
Hs Code.:

(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

Synonyms:(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

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Chemical Property of (S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

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Technology Process of (S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

There total 7 articles about (S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid 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: 74.0%

: 161878-71-3
di-tert-butyl L-γ-glutamyl-L-alanidate

: 4--N-ethylamino>benzoic acid trifluoroacetate salt

: 161878-87-1
(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

Guidance literature:: With diethyl cyanophosphoridate; triethylamine; In N,N-dimethyl-formamide; for 2h; Ambient temperature;
DOI:10.1021/jm00046a014

Reference yield:

: 5891-45-2
(S)-2-(benzyloxycarbonylamino)pentanedioic acid tert-butyl ester

: 161878-87-1
(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) isobutyl chloroformate, 4-methylmorpholine, / 1.) THF, -20 deg C, 10 min, 2.) THF, a) -20 deg C, 10 min, b) from -20 deg C toRT

2: 96 percent / H₂ / 10percent Pd/C / tetrahydrofuran / 4 h / 760 Torr

3: 74 percent / diethyl cyanophosphoridate, Et₃N / dimethylformamide / 2 h / Ambient temperature

With 4-methyl-morpholine; diethyl cyanophosphoridate; hydrogen; triethylamine; isobutyl chloroformate; palladium on activated charcoal; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm00046a014

Reference yield:

: 13404-22-3
tert-butyl L-alaninate hydrochloride

: 161878-87-1
(S)-4-((S)-1-tert-Butoxycarbonyl-ethylcarbamoyl)-2-{4-[ethyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-benzoylamino}-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) isobutyl chloroformate, 4-methylmorpholine, / 1.) THF, -20 deg C, 10 min, 2.) THF, a) -20 deg C, 10 min, b) from -20 deg C toRT

2: 96 percent / H₂ / 10percent Pd/C / tetrahydrofuran / 4 h / 760 Torr

3: 74 percent / diethyl cyanophosphoridate, Et₃N / dimethylformamide / 2 h / Ambient temperature

With 4-methyl-morpholine; diethyl cyanophosphoridate; hydrogen; triethylamine; isobutyl chloroformate; palladium on activated charcoal; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm00046a014