2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

Base Information

Chemical Name:2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide
CAS No.:1418759-13-3
Molecular Formula:C₂₃H₂₃ClN₆O₃
Molecular Weight:466.927
Hs Code.:

Synonyms:2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

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Chemical Property of 2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

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Technology Process of 2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

There total 6 articles about 2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-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: 19.0%

: 1418759-38-2
4-(3-chloro-4-methoxybenzyloxy)-2-(methylsulfinyl)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

: 73799-64-1
3-Azabicyclo<3.1.0>hexane hydrochloride

: 1418759-13-3
2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Cooling with ice;

Reference yield:

: 1418759-33-7
ethyl 4-(3-chloro-4-methoxybenzyloxy)-2-(methylmercapto)pyrimidine-5-carboxylate

: 1418759-13-3
2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide; water / tetrahydrofuran / 5 h / 20 °C

2: HATU; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C / Cooling with ice

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 12 h / 20 °C

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

With water; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; sodium hydroxide; In tetrahydrofuran; dichloromethane;

Reference yield:

: 1418759-34-8
4-(3-chloro-4-methoxybenzyloxy)-2-(methylmercapto)pyrimidine-5-carboxylic acid

: 1418759-13-3
2-(3-azadicyclo[3.1.0]hexan-3-yl)-4-(3-chloro-4-methoxybenzyloxy)-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: HATU; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C / Cooling with ice

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 12 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

With N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; In tetrahydrofuran; dichloromethane;