N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

Base Information

Chemical Name:N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide
CAS No.:1383579-47-2
Molecular Formula:C₂₀H₁₇N₅O₅S₂
Molecular Weight:471.517
Hs Code.:

Synonyms:N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

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Chemical Property of N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

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Technology Process of N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

There total 3 articles about N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide 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: 82.0%

: 1383579-32-5
4-amino-5-(hydroxymethyl)-2-(methylthio)furo[2,3-d]pyrimidine

: 1576-44-9
N-nosylaniline

: 1383579-47-2
N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

Guidance literature:: N-nosylaniline; With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 ℃; for 0.166667h;

4-amino-5-(hydroxymethyl)-2-(methylthio)furo[2,3-d]pyrimidine; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1055/s-0031-1290524

Reference yield:

: 62-53-3
aniline

: 1383579-47-2
N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere

2.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0.17 h / 0 °C

2.2: 0 - 20 °C

With pyridine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; 2.1: Mitsunobu reaction / 2.2: Mitsunobu reaction;
DOI:10.1055/s-0031-1290524

Reference yield:

: 1198054-16-8
ethyl 4-amino-2-(methylthio)furo[2,3-d]pyrimidine-5-carboxylate

: 1383579-47-2
N-({4-amino-2-(methylthio)furo[2,3-d]pyrimidin-5-yl}methyl)-4-nitro-N-phenylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / -50 - 20 °C

2.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0.17 h / 0 °C

2.2: 0 - 20 °C

With lithium aluminium tetrahydride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 2.1: Mitsunobu reaction / 2.2: Mitsunobu reaction;
DOI:10.1055/s-0031-1290524