(3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

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Chemical Name:(3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate
CAS No.:1541198-88-2
Molecular Formula:C₂₇H₃₅BrN₆O₅
Molecular Weight:603.516
Hs Code.:

Synonyms:(3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

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Chemical Property of (3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

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Technology Process of (3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

There total 12 articles about (3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate 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:

: 247102-01-8
5-N-(5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)-5-amino-nicotinic acid

: 1541197-63-0
(S)-3-(2-aminoacetylamino)-3-(3-bromo-5-tert-butylphenyl)propionic acid ethyl ester hydrochloride salt

: 1541198-88-2
(3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

Guidance literature:: 5-N-(5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)-5-amino-nicotinic acid; (S)-3-(2-aminoacetylamino)-3-(3-bromo-5-tert-butylphenyl)propionic acid ethyl ester hydrochloride salt; With benzotriazol-1-ol; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 0.166667h; Inert atmosphere;

With diisopropyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere;

Reference yield:

: 24242-19-1
5-aminonicotinic acid

: 1541198-88-2
(3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetonitrile / 12 h / 20 °C

2.1: sodium methylate / methanol / 1 h / 20 °C

3.1: N,N-dimethyl-formamide / 1 h / 20 °C

4.1: N,N-dimethyl-formamide / 5 h / Reflux

5.1: benzotriazol-1-ol / N,N-dimethyl-formamide; dichloromethane / 0.17 h / 20 °C / Inert atmosphere

5.2: 20 °C / Inert atmosphere

With sodium methylate; benzotriazol-1-ol; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 247102-02-9
N-(benzoyl)-N'-(3-carboxy-5-pyridinyl)thiourea

: 1541198-88-2
(3S)-ethyl 3-(3-bromo-5-(tert-butyl)phenyl)-3-(2-(5-((5-hydroxy-1,4,5,6-tetrahydropyrimidin-2-yl)amino)nicotinamido)acetamido)propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium methylate / methanol / 1 h / 20 °C

2.1: N,N-dimethyl-formamide / 1 h / 20 °C

3.1: N,N-dimethyl-formamide / 5 h / Reflux

4.1: benzotriazol-1-ol / N,N-dimethyl-formamide; dichloromethane / 0.17 h / 20 °C / Inert atmosphere

4.2: 20 °C / Inert atmosphere

With sodium methylate; benzotriazol-1-ol; In methanol; dichloromethane; N,N-dimethyl-formamide;