2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

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Chemical Name:2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine
CAS No.:1361960-85-1
Molecular Formula:C₂₃H₁₉FN₆OS
Molecular Weight:446.508
Hs Code.:

Synonyms:2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

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Chemical Property of 2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

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Technology Process of 2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

There total 2 articles about 2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-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:

: 1361960-93-1
2-(4-fluorophenylthio)-7H-pyrrolo[2,3-d]pyrimidin-4-ol

: 1361960-85-1
2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / 1 h / 110 °C

2: sodium t-butanolate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 15 h / 90 °C

With sodium t-butanolate; trichlorophosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In toluene;

Reference yield:

: 67831-83-8
2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidin-4-ol

: 1361960-85-1
2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: 3-chloro-benzenecarboperoxoic acid / N,N-dimethyl-formamide / 75 h / 0 - 20 °C

1.2: 20 h / 20 °C

2.1: trichlorophosphate / 1 h / 110 °C

3.1: sodium t-butanolate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 15 h / 90 °C

With 3-chloro-benzenecarboperoxoic acid; sodium t-butanolate; trichlorophosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In N,N-dimethyl-formamide; toluene;

Reference yield: 91.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 1361960-85-1
2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine

: 1361960-89-5
tert-butyl-2-(4-fluorophenylthio)-7H-pyrrolo[2,3-d]pyrimidin-4-yl-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)carbamate

Guidance literature:: di-tert-butyl dicarbonate; 2-(4-fluorophenylthio)-N-(1-(4-methoxybenzyl)-1H-pyrazol-5-yl)-7H-pyrrolo[2,3-d]pyrimidine-4-amine; With potassium carbonate; dmap; In 1,4-dioxane; at 40 ℃; for 2h;

With ammonium hydroxide; In 1,4-dioxane; methanol; at 20 ℃; for 3h;