4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

Base Information

Chemical Name:4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide
CAS No.:1283690-30-1
Molecular Formula:C₃₀H₃₃F₃N₆O₄
Molecular Weight:598.625
Hs Code.:

Synonyms:4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

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Chemical Property of 4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

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Technology Process of 4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

There total 5 articles about 4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide 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:

: 1226992-79-5
4-(4-chloro-5-trifluoromethyl-pyrimidin-2-ylamino)-3-methoxy-N-(1-methyl-prperidin-4-yl)-benzamide

: 108-24-7
acetic anhydride

: 1283690-30-1
4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

Guidance literature:: With caesium carbonate; In 1,4-dioxane; at 85 ℃;

Reference yield:

: 41838-46-4
4-Amino-1-methylpiperidine

: 1283690-30-1
4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / toluene / 2 h / 120 °C

1.2: 0 - 20 °C

2.1: caesium carbonate / 1,4-dioxane / 85 °C

With thionyl chloride; caesium carbonate; In 1,4-dioxane; toluene;

Reference yield:

: 869937-03-1
4-{[4-chloro-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-methoxybenzoic acid

: 1283690-30-1
4-[4-((1R,2R)-1-acetylamino-indan-2-yloxy)-5-trifluoromethyl-pyrimidin-2-ylamino]-3-methoxy-N-(1-methyl-piperidin-4-yl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / toluene / 2 h / 120 °C

1.2: 0 - 20 °C

2.1: caesium carbonate / 1,4-dioxane / 85 °C

With thionyl chloride; caesium carbonate; In 1,4-dioxane; toluene;