N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

Base Information

Chemical Name:N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate
CAS No.:1005195-59-4
Molecular Formula:C₂HF₃O₂*C₂₇H₂₅ClN₆O₂
Molecular Weight:615.011
Hs Code.:

Synonyms:N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

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Chemical Property of N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

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Technology Process of N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

There total 5 articles about N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate 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:

: 1005195-57-2
tert-butyl 4-(2-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino) quinazolin-6-ylamino)-2-oxoethylidene) piperidine-1-carboxylate

: 76-05-1
trifluoroacetic acid

: 1005195-59-4
N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

Guidance literature:: In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 193085-24-4
4-carboxymethylenepiperidine-1-carboxylic acid tert-butyl ester

: 1005195-59-4
N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.33 h / 0 °C

1.2: 0 °C

2.1: dichloromethane / 2 h / 20 °C

With 4-methyl-morpholine; isobutyl chloroformate; In tetrahydrofuran; dichloromethane;

Reference yield:

: 41979-39-9
4-piperidone hydrochloride

: 1005195-59-4
N-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-6-yl)-2-(piperidin-4-ylidene)acetamide trifluoroacetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydrogencarbonate; sodium chloride / tetrahydrofuran; water / 20 °C

2.1: sodium hydroxide / ethanol / 0.5 h / 20 °C

2.2: 20 °C

2.3: pH 4

3.1: lithium hydroxide; water / tetrahydrofuran; methanol / 20 °C

3.2: pH 4

4.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.33 h / 0 °C

4.2: 0 °C

5.1: dichloromethane / 2 h / 20 °C

With 4-methyl-morpholine; lithium hydroxide; sodium hydroxide; water; sodium hydrogencarbonate; sodium chloride; isobutyl chloroformate; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;