4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

Base Information

Chemical Name:4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide
CAS No.:934328-22-0
Molecular Formula:C₂₁H₃₁N₇O₃
Molecular Weight:429.522
Hs Code.:

Synonyms:4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

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Chemical Property of 4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

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Technology Process of 4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

There total 5 articles about 4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-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:

: 4-{[(1S,2R)-2-(cyanoamino)cyclohexyl]amino}-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

: O-methyl hydroxylamine hydrochloride

: 934328-22-0
4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

Guidance literature:: With sodium carbonate; In ethanol; for 1h; Reflux;

Reference yield:

: 620957-84-8
ethyl 4-({(1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclohexyl}amino)-6-methylquinazolin-2-carboxylate

: 934328-22-0
4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: methanol / di-isopropyl ether / 15.5 h / 0 - 50 °C

2: hydrogenchloride / ethyl acetate; diethyl ether / 48.5 h / 20 °C

3: triethylamine / tetrahydrofuran / 0.5 h / -20 °C / Inert atmosphere

4: sodium carbonate / ethanol / 1 h / Reflux

With hydrogenchloride; methanol; sodium carbonate; triethylamine; In tetrahydrofuran; diethyl ether; ethanol; di-isopropyl ether; ethyl acetate;

Reference yield:

: 934301-48-1
4-{[(1S,2R)-2-aminocyclohexyl]amino}-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

: 934328-22-0
4-[((1S,2R)-2-{[amino(methoxyimino)methyl]amino}cyclohexyl)amino]-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0.5 h / -20 °C / Inert atmosphere

2: sodium carbonate / ethanol / 1 h / Reflux

With sodium carbonate; triethylamine; In tetrahydrofuran; ethanol;