(E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

Base Information

Chemical Name:(E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester
CAS No.:1027480-77-8
Molecular Formula:C₂₈H₃₀ClN₃O₅S
Molecular Weight:556.082
Hs Code.:

Synonyms:(E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

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Chemical Property of (E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

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Technology Process of (E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

There total 7 articles about (E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester 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:

: 144-48-9
iodacetamide

: 153732-13-9
(E)-methyl 6-[4-(2-{[(4-chlorophenyl)sulfonyl]amino}ethyl)phenyl]-6-( 3-pyridyl)hex-5-enoate

: 1027480-77-8
(E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

Guidance literature:: With potassium tert-butylate; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

Reference yield:

: 877-95-2
methyl-N-(benzyl-methyl)-formamide

: 1027480-77-8
(E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) AlCl₃, 2.) 6 N aq. HCl, 3.) 10 N NaHCO₃, NaOH

2: 75 percent / potassium tert-butoxide / tetrahydrofuran / 1.5 h / -20 - 10 °C

3: 81 percent / HCl / 2 h / Heating

4: potassium tert-butoxide / dimethylformamide / 1 h / 20 °C

With hydrogenchloride; sodium hydroxide; aluminium trichloride; potassium tert-butylate; sodium hydrogencarbonate; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 17814-85-6
(4-carboxybutyl)triphenylphosphonium bromide

: 1027480-77-8
(E)-6-(4-{2-[Carbamoylmethyl-(4-chloro-benzenesulfonyl)-amino]-ethyl}-phenyl)-6-pyridin-3-yl-hex-5-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / potassium tert-butoxide / tetrahydrofuran / 1.5 h / -20 - 10 °C

2: 81 percent / HCl / 2 h / Heating

3: potassium tert-butoxide / dimethylformamide / 1 h / 20 °C

With hydrogenchloride; potassium tert-butylate; In tetrahydrofuran; N,N-dimethyl-formamide;