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C37H48N6O8S

Base Information
  • Chemical Name:C37H48N6O8S
  • CAS No.:1610955-24-2
  • Molecular Formula:C37H48N6O8S
  • Molecular Weight:736.89
  • Hs Code.:
C<sub>37</sub>H<sub>48</sub>N<sub>6</sub>O<sub>8</sub>S

Synonyms:C37H48N6O8S

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Chemical Property of C37H48N6O8S
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Technology Process of C37H48N6O8S

There total 13 articles about C37H48N6O8S 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:
Guidance literature:
Multi-step reaction with 13 steps
1.1: oxalyl dichloride; dmap / dichloromethane / 20 °C
2.1: triethylamine / dichloromethane / 0 - 20 °C
3.1: tetrahydrofuran / 2 h / 20 °C
4.1: triethylsilane; boron trifluoride diethyl etherate / acetonitrile / 2 h / 0 - 60 °C
5.1: tert-butylmagnesium chloride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere
5.2: 1.5 h / -78 - 60 °C
6.1: sodium tetrahydroborate; cerium(III) chloride heptahydrate; methanol; water; sodium hydroxide / 0.25 h
7.1: water; acetic acid / 7 h / 100 °C
8.1: dmap; triethylamine / acetonitrile / 1 h / 20 °C
9.1: thiourea; trimethylsilyl trifluoromethanesulfonate / 1,4-dioxane / 3 h / 80 °C
9.2: 18 h / 20 °C
10.1: tri tert-butylphosphoniumtetrafluoroborate; N-Methyldicyclohexylamine; tris-(dibenzylideneacetone)dipalladium(0) / 1-methyl-pyrrolidin-2-one / 0.33 h / 160 °C / Microwave irradiation
11.1: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 2068.65 Torr
12.1: trimethylsilylazide; di(n-butyl)tin oxide / toluene / 18 h / 90 °C
13.1: triethylamine / acetonitrile / 18 h / 60 °C
With methanol; triethylsilane; dmap; sodium tetrahydroborate; tris-(dibenzylideneacetone)dipalladium(0); oxalyl dichloride; trimethylsilyl trifluoromethanesulfonate; cerium(III) chloride heptahydrate; trimethylsilylazide; N-Methyldicyclohexylamine; palladium 10% on activated carbon; boron trifluoride diethyl etherate; tert-butylmagnesium chloride; water; hydrogen; di(n-butyl)tin oxide; acetic acid; triethylamine; thiourea; sodium hydroxide; tri tert-butylphosphoniumtetrafluoroborate; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 10 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
9.1: trimethylsilylazide; di(n-butyl)tin oxide / toluene / 18 h / 90 °C
10.1: triethylamine / acetonitrile / 18 h / 60 °C
With methanol; triethylsilane; dmap; sodium tetrahydroborate; tris-(dibenzylideneacetone)dipalladium(0); trimethylsilyl trifluoromethanesulfonate; cerium(III) chloride heptahydrate; trimethylsilylazide; N-Methyldicyclohexylamine; palladium 10% on activated carbon; boron trifluoride diethyl etherate; tert-butylmagnesium chloride; water; hydrogen; di(n-butyl)tin oxide; acetic acid; triethylamine; thiourea; sodium hydroxide; tri tert-butylphosphoniumtetrafluoroborate; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; toluene; acetonitrile;
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