2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

Base Information

Chemical Name:2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide
CAS No.:1194960-91-2
Molecular Formula:C₁₉H₂₂BrN₉O
Molecular Weight:472.347
Hs Code.:

Synonyms:2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

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Chemical Property of 2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

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Technology Process of 2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

There total 6 articles about 2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide 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:

: 1236187-89-5
tert-butyl (1S,2R)-2-(4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)-5-carbamoylpyrimidin-2-ylamino)cyclohexylcarbamate

: 1194960-91-2
2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

Guidance literature:: With trifluoroacetic acid;

Reference yield:

: 1370261-93-0
ethyl 4-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-2-(methylthio)pyrimidine-5-carboxylate

: 1194960-91-2
2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hydroxide monohydrate / 1,4-dioxane; water

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2.5 h

2.2: 2 h

3.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 1.2 h

3.2: 3 h / 90 °C

4.1: trifluoroacetic acid

With N-Bromosuccinimide; lithium hydroxide monohydrate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 1370261-94-1
C₁₄H₁₂N₆O₂S

: 1194960-91-2
2-((1R,2S)-2-aminocyclohexylamino)-4-(3-bromo-5-(2H-1,2,3-triazol-2-yl)phenylamino)pyrimidin-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2.5 h

1.2: 2 h

2.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 1.2 h

2.2: 3 h / 90 °C

3.1: trifluoroacetic acid

With N-Bromosuccinimide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In N,N-dimethyl-formamide;