(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester
CAS No.:406229-95-6
Molecular Formula:C₃₇H₄₉N₅O₇S₂
Molecular Weight:739.957
Hs Code.:

(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

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Chemical Property of (5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

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Technology Process of (5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

There total 12 articles about (5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl 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:

: 406233-26-9
4-(4,4-dimethylpiperidin-1-yl)benzoic acid

: 406233-48-5
((R)-5-(2-nitro-4-sulfamoylphenylamino)-6-phenylsulfanylhexyl)carbamic acid tert-butyl ester

: 406229-95-6
(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/jm050754u

Reference yield:

: 406233-31-6
4-fluoro-3-nitrobenzenesulfonamide

: 406229-95-6
(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: DIPEA / dimethylformamide / 12 h / 20 °C

2: EDCI; DMAP / CH₂Cl₂ / 24 h / 20 °C

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm050754u

Reference yield:

: 406233-25-8
ethyl 4-(4,4-dimethylpiperidin-1-yl)benzoate

: 406229-95-6
(5-{4-[4-(4,4-dimethyl-piperidin-1-yl)-benzoylsulfamoyl]-2-nitro-phenylamino}-6-phenylsulfanyl-hexyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / aq. LiOH / tetrahydrofuran; methanol / 18 h / 20 °C

2: EDCI; DMAP / CH₂Cl₂ / 24 h / 20 °C

With dmap; lithium hydroxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm050754u