N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

Base Information

Chemical Name:N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide
CAS No.:1125632-75-8
Molecular Formula:C₁₆H₁₃ClN₄O₂S
Molecular Weight:360.824
Hs Code.:

Synonyms:N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

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Chemical Property of N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

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Technology Process of N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

There total 7 articles about N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide 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: 75.0%

: 1125632-74-7
N-(5-{4-chloro-3-[(trifluoroacetyl)amino]phenoxy}[1,3]-thiazolo[5,4-b]pyridin-2-yl)cyclopropanecarboxamide

: 1125632-75-8
N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

Guidance literature:: N-(5-{4-chloro-3-[(trifluoroacetyl)amino]phenoxy}[1,3]-thiazolo[5,4-b]pyridin-2-yl)cyclopropanecarboxamide; With methanol; sodium tetrahydroborate; ethanol; at 20 ℃; for 1h; Cooling;

With water; In methanol; ethanol; ethyl acetate;

Reference yield:

: 16026-77-0
3-amino-4-chlorophenol

: 1125632-75-8
N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C

2: tetrahydrofuran / 1 h / 20 °C

3: acetic acid; iron / 3 h / 60 °C

4: bromine; acetic acid / 16 h / 20 °C / Cooling with ice

5: pyridine / 1 h / 20 °C / Cooling with ice

6: ethanol; sodium tetrahydroborate; methanol / 1 h / 20 °C / Cooling

With pyridine; methanol; sodium tetrahydroborate; ethanol; bromine; iron; potassium carbonate; acetic acid; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 1125632-75-8
N-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C

2: tetrahydrofuran / 1 h / 20 °C

3: acetic acid; iron / 3 h / 60 °C

4: bromine; acetic acid / 16 h / 20 °C / Cooling with ice

5: pyridine / 1 h / 20 °C / Cooling with ice

6: ethanol; sodium tetrahydroborate; methanol / 1 h / 20 °C / Cooling

With pyridine; methanol; sodium tetrahydroborate; ethanol; bromine; iron; potassium carbonate; acetic acid; In tetrahydrofuran; N,N-dimethyl-formamide;