(3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

Base Information

Chemical Name:(3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide
CAS No.:1435953-16-4
Molecular Formula:C₁₉H₂₃N₇O₂S
Molecular Weight:413.503
Hs Code.:

Synonyms:(3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

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Chemical Property of (3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

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Technology Process of (3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

There total 5 articles about (3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-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:

: 1435953-84-6
7-[(2S)-2-methylpiperazin-1-yl]thiazolo[5,4-d]pyrimidin-5-amine hydrochloride

: 60385-06-0
1-isocyanato-4-methoxy-2-methylbenzene

: 1435953-16-4
(3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 48h;

Reference yield:

: 171887-03-9
N-(2-amino-4,6-dichloropyrimidin-5-yl)formamide

: 1435953-16-4
(3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: Lawessons reagent / tetrahydrofuran / 0.5 h / 65 °C

2: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 0.75 h / 120 °C / Microwave irradiation

3: hydrogenchloride / 1,4-dioxane / 12 h / 20 °C

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 48 h / 20 °C

With Lawessons reagent; hydrogenchloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;

Reference yield:

: 1211527-74-0
7-chlorothiazolo[5,4-d]pyrimidin-5-amine

: 1435953-16-4
(3S)-4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-N-(4-methoxy-2-methyl-phenyl)-3-methyl-piperazine-1-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 0.75 h / 120 °C / Microwave irradiation

2: hydrogenchloride / 1,4-dioxane / 12 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 48 h / 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane;