5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

Base Information

Chemical Name:5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride
CAS No.:1182402-92-1
Molecular Formula:C₃₁H₃₄ClFN₂O₆S*ClH
Molecular Weight:653.599
Hs Code.:

5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

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Chemical Property of 5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

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Technology Process of 5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

There total 6 articles about 5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride 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:

: 1182402-94-3
tert-butyl 4-[3-[5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluoro-phenyl)-6-methoxy-2-oxo-2,3-dihydro-1H-indol-3-yl]propyl]piperidin-1-carboxylate

: 1182402-92-1,1182402-93-2,1182402-95-4
5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether; at 20 ℃; for 16h;

Reference yield:

: 84478-76-2
1-chloro-5-fluoro-2-methoxy-4-nitrobenzene

: 1182402-92-1,1182402-93-2,1182402-95-4
5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / -20 - 3 °C

2.1: acetic acid; iron / methanol / 16 h / Reflux

3.1: potassium tert-butylate / N,N-dimethyl-formamide / -40 - -15 °C / Inert atmosphere

3.2: 16 h / -50 - 12 °C

4.1: potassium tert-butylate / tetrahydrofuran / -30 - 0 °C

4.2: -60 - 20 °C

5.1: hydrogenchloride / diethyl ether / 16 h / 20 °C

With hydrogenchloride; potassium tert-butylate; iron; sodium hydride; acetic acid; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 57486-67-6
methyl o-fluorophenylacetate

: 1182402-92-1,1182402-93-2,1182402-95-4
5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-fluorophenyl)-6-methoxy-3-(3-(piperidin-4-yl)propyl)-1,3-dihydro-2H-indol-2-one hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / -20 - 3 °C

2.1: acetic acid; iron / methanol / 16 h / Reflux

3.1: potassium tert-butylate / N,N-dimethyl-formamide / -40 - -15 °C / Inert atmosphere

3.2: 16 h / -50 - 12 °C

4.1: potassium tert-butylate / tetrahydrofuran / -30 - 0 °C

4.2: -60 - 20 °C

5.1: hydrogenchloride / diethyl ether / 16 h / 20 °C

With hydrogenchloride; potassium tert-butylate; iron; sodium hydride; acetic acid; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide; mineral oil;