C₃₀H₃₅NO₇S

Base Information

Chemical Name:C₃₀H₃₅NO₇S
CAS No.:1610955-21-9
Molecular Formula:C₃₀H₃₅NO₇S
Molecular Weight:553.676
Hs Code.:

C<sub>30</sub>H<sub>35</sub>NO<sub>7</sub>S

Synonyms:C₃₀H₃₅NO₇S

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Chemical Property of C₃₀H₃₅NO₇S

Chemical Property:

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Technology Process of C₃₀H₃₅NO₇S

There total 11 articles about C₃₀H₃₅NO₇S 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:

: 1610955-19-5
(2S,3S,4R,5S,6R)-2-(3-(4-((E)-3-cyanoprop-1-en-1-yl)benzyl)-4-methylphenyl)-6-(methylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

: 1610955-21-9
C₃₀H₃₅NO₇S

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; for 5h; under 2068.65 Torr;

Reference yield:

: 1500921-65-2
(5-bromo-2-methylphenyl)(4-chlorophenyl)methanone

: 1610955-21-9
C₃₀H₃₅NO₇S

Guidance literature:: Multi-step reaction with 8 steps

1.1: triethylsilane; boron trifluoride diethyl etherate / acetonitrile / 2 h / 0 - 60 °C

2.1: tert-butylmagnesium chloride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

2.2: 1.5 h / -78 - 60 °C

3.1: sodium tetrahydroborate; cerium(III) chloride heptahydrate; methanol; water; sodium hydroxide / 0.25 h

4.1: water; acetic acid / 7 h / 100 °C

5.1: dmap; triethylamine / acetonitrile / 1 h / 20 °C

6.1: thiourea; trimethylsilyl trifluoromethanesulfonate / 1,4-dioxane / 3 h / 80 °C

6.2: 18 h / 20 °C

7.1: tri tert-butylphosphoniumtetrafluoroborate; N-Methyldicyclohexylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1-methyl-pyrrolidin-2-one / 0.33 h / 160 °C / Microwave irradiation

8.1: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 2068.65 Torr

With methanol; triethylsilane; dmap; sodium tetrahydroborate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trimethylsilyl trifluoromethanesulfonate; cerium(III) chloride heptahydrate; N-Methyldicyclohexylamine; palladium 10% on activated carbon; boron trifluoride diethyl etherate; tert-butylmagnesium chloride; water; hydrogen; acetic acid; triethylamine; thiourea; sodium hydroxide; tri tert-butylphosphoniumtetrafluoroborate; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; acetonitrile;

Reference yield:

: 1610954-86-3
(3-(4-chlorobenzyl)-4-methylphenyl)((3aS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanone

: 1610955-21-9
C₃₀H₃₅NO₇S

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium tetrahydroborate; cerium(III) chloride heptahydrate; methanol; water; sodium hydroxide / 0.25 h

2.1: water; acetic acid / 7 h / 100 °C

3.1: dmap; triethylamine / acetonitrile / 1 h / 20 °C

4.1: thiourea; trimethylsilyl trifluoromethanesulfonate / 1,4-dioxane / 3 h / 80 °C

4.2: 18 h / 20 °C

5.1: tri tert-butylphosphoniumtetrafluoroborate; N-Methyldicyclohexylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1-methyl-pyrrolidin-2-one / 0.33 h / 160 °C / Microwave irradiation

6.1: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 2068.65 Torr

With methanol; dmap; sodium tetrahydroborate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trimethylsilyl trifluoromethanesulfonate; cerium(III) chloride heptahydrate; N-Methyldicyclohexylamine; palladium 10% on activated carbon; water; hydrogen; acetic acid; triethylamine; thiourea; sodium hydroxide; tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; acetonitrile;