(S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

Base Information

Chemical Name:(S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide
CAS No.:1426336-93-7
Molecular Formula:C₂₁H₂₀FN₅O₄
Molecular Weight:425.419
Hs Code.:

Synonyms:(S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

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Chemical Property of (S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

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Technology Process of (S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

There total 9 articles about (S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-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:

: 1426336-92-6
(S)-methyl 5-(4-((1-amino-1-oxopropan-2-yl)amino)-6-carbamoylpyrimidin-2-yl)-2-(4-fluorophenoxy)benzoate

: 1426336-93-7
(S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

Guidance literature:: With sodium tetrahydroborate; ethanol; at 20 ℃; for 2h;

Reference yield:

: 1426337-12-3
(S)-methyl 2-chloro-6-((1-methoxy-1-oxopropan-2-yl)amino)pyrimidine-4-carboxylate

: 1426336-93-7
(S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: ammonia / methanol / 72 h / 50 °C / Sealed tube

2: caesium carbonate; water; bis-triphenylphosphine-palladium(II) chloride / ethanol; 1,2-dimethoxyethane / 3 h / 80 °C / Sealed tube; Inert atmosphere

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene / dichloromethane / 2 h / 20 °C

4: caesium carbonate / N,N-dimethyl-formamide / 96 h / 65 °C

5: sodium tetrahydroborate / ethanol / 2 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; sodium tetrahydroborate; ammonia; water; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 6299-85-0
2,6-dichloropyrimidine-4-carboxylic acid methyl ester

: 1426336-93-7
(S)-6-((1-amino-1-oxopropan-2-yl)amino)-2-(4-(4-fluorophenoxy)-3-(hydroxymethyl)phenyl)pyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 50 °C

2: ammonia / methanol / 72 h / 50 °C / Sealed tube

3: caesium carbonate; water; bis-triphenylphosphine-palladium(II) chloride / ethanol; 1,2-dimethoxyethane / 3 h / 80 °C / Sealed tube; Inert atmosphere

4: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene / dichloromethane / 2 h / 20 °C

5: caesium carbonate / N,N-dimethyl-formamide / 96 h / 65 °C

6: sodium tetrahydroborate / ethanol / 2 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; sodium tetrahydroborate; ammonia; water; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;