N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

Base Information

Chemical Name:N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide
CAS No.:1357176-18-1
Molecular Formula:C₂₇H₃₀N₂O₅S
Molecular Weight:494.612
Hs Code.:

Synonyms:N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

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Chemical Property of N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

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Technology Process of N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

There total 7 articles about N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide 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:

: 1316759-24-6
4-[4-[2-[(3S)-3-hydroxyquinuclidin-3-yl]ethynyl]phenoxy]benzoic acid

: 117593-43-8
(+/-)-3-aminotetrahydrothiopyran-1,1-dioxide

: 1357176-18-1
N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 - 24 ℃; for 3h;
DOI:10.1016/j.bmcl.2011.11.034

Reference yield:

: 1316759-21-3
methyl 4-[4-[2-[(3S)-3-hydroxyquinuclidin-3-yl]ethynyl]phenoxy]benzoate

: 1357176-18-1
N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: water; sodium hydroxide / methanol / 2.5 h / 50 °C

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 3 h / 20 - 24 °C

With water; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.11.034

Reference yield:

: 1344839-90-2
dihydro-2H-thiopyran-3(4H)-one 1,1-dioxide oxime

: 1357176-18-1
N-(1,1-dioxothian-3-yl)-4-[4-[2-[(5S)-5-hydroxy-1-azabicyclo[2.2.2]oct-5-yl]ethynyl]phenoxy]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 20 h / 0 - 50 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 3 h / 20 - 24 °C

With lithium aluminium tetrahydride; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.11.034