4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide

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Chemical Name:4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide
CAS No.:1610549-12-6
Molecular Formula:C₃₃H₂₈N₈O₃S₂
Molecular Weight:648.769
Hs Code.:

Synonyms:4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide

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Chemical Property of 4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide

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Technology Process of 4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide

There total 2 articles about 4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide 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: 46.0%

: 68-35-9
sulfadiazine

: 1610549-49-9
5,6-diphenyl-4-piperazin-1-ylfuro[2,3-d]pyrimidine

: 1610549-12-6
4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide

Guidance literature:: 5,6-diphenyl-4-piperazin-1-ylfuro[2,3-d]pyrimidine; With 1,1'-Thiocarbonyldiimidazole; In dichloromethane; at 20 ℃; for 14h; Inert atmosphere;

sulfadiazine; In dichloromethane; at 20 ℃; for 6h; Inert atmosphere;
DOI:10.1002/cmdc.201300571

Reference yield:

: 65148-07-4
4-chloro-5,6-diphenylfuro[2,3-d]pyrimidine

: 1610549-12-6
4-(5,6-diphenylfuro[2,3-d]pyrimidin-4-yl)-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}piperazine-1-carbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: ethanol / 8 h / 80 °C / Inert atmosphere

2.1: 1,1'-Thiocarbonyldiimidazole / dichloromethane / 14 h / 20 °C / Inert atmosphere

2.2: 6 h / 20 °C / Inert atmosphere

With 1,1'-Thiocarbonyldiimidazole; In ethanol; dichloromethane;
DOI:10.1002/cmdc.201300571