S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

Base Information

Chemical Name:S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate
CAS No.:1608082-75-2
Molecular Formula:C₂₈H₂₇F₃IN₇O₂S₂
Molecular Weight:741.6
Hs Code.:

Synonyms:S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

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Chemical Property of S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

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Technology Process of S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

There total 2 articles about S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate 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: 77.0%

: 1629496-67-8
C₁₃H₁₅N₃OS₂

: 1608082-45-6
N-allyl-N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamide

: 1608082-75-2
S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

Guidance literature:: With dilauryl peroxide; In ethyl acetate; for 0.5h; Inert atmosphere; Reflux;
DOI:10.1021/ol500985f

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 1608082-75-2
S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / 120 h / 0 - 20 °C / Inert atmosphere

2: tetrahydrofuran / 96 h / Reflux; Inert atmosphere

3: dichloromethane / 3 h / Inert atmosphere; Reflux

4: dilauryl peroxide / ethyl acetate / 0.5 h / Inert atmosphere; Reflux

With dilauryl peroxide; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/ol500985f

Reference yield: 26.0%

: 1608082-75-2
S-(4-(1-benzyl-1H-tetrazol-5-yl)-1-(N-(3,5,6-trifluoro-4-((4-iodophenyl)amino)pyridin-2-yl)acetamido)butan-2-yl) O-ethyl carbonodithioate

: 1-(3-(2-(1-benzyl-1H-tetrazol-5-yl)ethyl)-5,6-difluoro-4-((4-iodophenyl)amino)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-1-yl)ethanone

Guidance literature:: With 2,6-dimethylpyridine; di-tert-butyl peroxide; In chlorobenzene; for 3h; Inert atmosphere; Reflux;
DOI:10.1021/ol500985f