5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

Base Information

Chemical Name:5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride
CAS No.:1068975-17-6
Molecular Formula:C₂₀H₁₃ClF₂N₄O₃S
Molecular Weight:462.864
Hs Code.:

Synonyms:5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

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Chemical Property of 5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

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Technology Process of 5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

There total 8 articles about 5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride 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:

: 1068975-16-5
5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonic acid

: 1068975-17-6
5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

Guidance literature:: With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 ℃; for 3h;

Reference yield:

: 399-52-0
5-fluoro-1H-indole

: 1068975-17-6
5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium tert-butylate / N,N-dimethyl-formamide / 2 h / 20 °C

1.2: 2.25 h / 20 °C

2.1: potassium carbonate / water; ethyl acetate / 20 °C

3.1: chlorosulfonic acid / acetonitrile / 2 h / 0 °C

4.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 3 h / 0 °C

With chlorosulfonic acid; oxalyl dichloride; potassium tert-butylate; potassium carbonate; N,N-dimethyl-formamide; In dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid ethyl ester

: 1068975-17-6
5-fluoro-1-{[2-(3-fluorophenyl)-4-methylpyrimidine-5-carbonyl]amino}-1H-indole-3-sulfonyl chloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: methanol; sodium hydroxide; water / tetrahydrofuran / 0.75 h / Heating / reflux

1.2: pH 2 - 3

2.1: N,N-diethyl-N-isopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 8 h / 20 - 80 °C

3.1: chlorosulfonic acid / acetonitrile / 2 h / 0 °C

4.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 3 h / 0 °C

With methanol; chlorosulfonic acid; sodium hydroxide; oxalyl dichloride; N,N-diethyl-N-isopropylamine; water; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile;