4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1374856-78-6
Molecular Formula:C₂₀H₂₉N₃O₆S
Molecular Weight:439.533
Hs Code.:

Synonyms:4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

There total 1 articles about 4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic 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: 61.0%

: 701298-37-5
tert-butyl 4-[(2-hydroxyethyl)amino]piperidine-1-carboxylate

: 439585-11-2
N-[[[(benzyloxy)carbonyl]azanide]sulfonyl]-N,N-diethylethylammonium

: 1374856-78-6
4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: In tetrahydrofuran; for 16h; Reflux;
DOI:10.1016/j.bmcl.2012.03.049

Reference yield: 64.0%

: 1374856-78-6
4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

: 76-05-1
trifluoroacetic acid

: 1374856-80-0
1,1-dioxo-5-piperidin-4-yl-1λ6-[1,2,5]thiadiazolidine-2-benzyl carboxylate trifluoroacetic acid salt

Guidance literature:: In dichloromethane; at 20 ℃; for 16h;
DOI:10.1016/j.bmcl.2012.03.049

Reference yield:

: 1374856-78-6
4-(5-benzyloxycarbonyl-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

: N-{2-[4-(1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-2-yl)-piperidin-1-yl]-4-methylquinazolin-6-yl}-3-(4-trifluoromethoxyphenyl)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: dichloromethane / 16 h / 20 °C

2: triethylamine / methanol / 2 h / Reflux

3: sodium hydroxide / tetrahydrofuran; water / 2 h / 20 °C

4: palladium 10% on activated carbon; hydrogen / ethanol / 2 h

5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 6 h / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2012.03.049