(R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

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Chemical Name:(R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine
CAS No.:1616371-85-7
Molecular Formula:C₂₇H₂₅ClF₃IN₄
Molecular Weight:624.875
Hs Code.:

Synonyms:(R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

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Chemical Property of (R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

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Technology Process of (R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

There total 6 articles about (R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine 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:

: 1616371-83-5
(R)-2-chloro-N-(1-cyclobutylethyl)-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

: 1616371-85-7
(R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Guidance literature:: With Iodine monochloride; In dichloromethane; at 0 - 25 ℃; for 2h;

Reference yield:

: 1338377-74-4
(S)-N-[(1E)-cyclobutylmethylidene]-2-methylpropane-2-sulfinamide

: 1616371-85-7
(R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran; diethyl ether / 6 h / -78 - -40 °C / Inert atmosphere

2: hydrogenchloride / methanol; 1,4-dioxane / 2 h / 0 - 25 °C

3: triethylamine / ethanol / 9 h / 70 - 80 °C / Sealed tube

4: Iodine monochloride / dichloromethane / 2 h / 0 - 25 °C

With hydrogenchloride; Iodine monochloride; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; dichloromethane;

Reference yield:

: 677743-79-2,1355969-30-0
(1R)-1-cyclobutylethan-1-amine hydrogen chloride salt

: 1616371-85-7
(R)-2-chloro-N-(1-cyclobutylethyl)-7-iodo-6-(m-tolyl)-5-(4-(trifluoromethyl)benzyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethanol / 9 h / 70 - 80 °C / Sealed tube

2: Iodine monochloride / dichloromethane / 2 h / 0 - 25 °C

With Iodine monochloride; triethylamine; In ethanol; dichloromethane;