(S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

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Chemical Name:(S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate
CAS No.:1449475-62-0
Molecular Formula:C₄₁H₃₆ClN₅O₃
Molecular Weight:682.222
Hs Code.:

Synonyms:(S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

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Chemical Property of (S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

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Technology Process of (S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

There total 3 articles about (S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate 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: 48.0%

: 677743-50-9
(2-chloro-4-cyanophenyl)boronic acid

: (S)-tert-butyl (1-(5-bromo-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

: 1449475-62-0
(S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In 1,2-dimethoxyethane; water; at 120 ℃; for 1h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 1575-37-7
4-Bromo-benzene-1,2-diamine

: 1449475-62-0
(S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 1 h / 0 °C

1.2: 4 h / 0 - 20 °C

1.3: 2 h / 65 °C

2.1: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; 1,2-dimethoxyethane / 1 h / 120 °C / Inert atmosphere; Microwave irradiation

With 4-methyl-morpholine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; isobutyl chloroformate; In tetrahydrofuran; 1,2-dimethoxyethane; water;

Reference yield:

: 132388-68-2
N^α-tert-butoxycarbonyl-N^ω-triphenylmethyl-L-asparagine

: 1449475-62-0
(S)-tert-butyl (1-(6-(2-chloro-4-cyanophenyl)-1H-benzo[d]imidazol-2-yl)-3-oxo-3-(tritylamino)propyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 1 h / 0 °C

1.2: 4 h / 0 - 20 °C

1.3: 2 h / 65 °C

2.1: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; 1,2-dimethoxyethane / 1 h / 120 °C / Inert atmosphere; Microwave irradiation

With 4-methyl-morpholine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; isobutyl chloroformate; In tetrahydrofuran; 1,2-dimethoxyethane; water;