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C36H33N3O7

Base Information
  • Chemical Name:C36H33N3O7
  • CAS No.:188028-00-4
  • Molecular Formula:C36H33N3O7
  • Molecular Weight:619.674
  • Hs Code.:
C<sub>36</sub>H<sub>33</sub>N<sub>3</sub>O<sub>7</sub>

Synonyms:C36H33N3O7

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Chemical Property of C36H33N3O7
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Technology Process of C36H33N3O7

There total 8 articles about C36H33N3O7 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:
With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol; for 16h;
DOI:10.1021/ja971304x
Guidance literature:
Multi-step reaction with 7 steps
1: 89 percent / LiBH4 / tetrahydrofuran / 0.33 h
2: 71 percent / pyridinium trifluoroacetate, 1,3-dicyclohexylcarbodiimide / benzene; dimethylsulfoxide / 9 h / Ambient temperature
3: 85 percent / BF3*OEt2 / diethyl ether / 24 h / 25 - 30 °C
4: 95 percent / NaBH4 / methanol; CH2Cl2; CHCl3 / 0.08 h
5: 1.) NaH / 1) THF, 25 min; 2) THF, 50 min
6: 88 percent / Martin's sulfurane / CDCl3 / 0.33 h
7: 84 percent / 4-methylmorpholine-N-oxide, OsO4 / 2-methyl-propan-2-ol; acetone; H2O / 16 h
With sodium tetrahydroborate; osmium(VIII) oxide; lithium borohydride; Martins sulfurane; boron trifluoride diethyl etherate; pyridinium trifluroacetate; sodium hydride; 4-methylmorpholine N-oxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; diethyl ether; chloroform-d1; dichloromethane; chloroform; water; dimethyl sulfoxide; acetone; tert-butyl alcohol; benzene;
DOI:10.1021/ja971304x
Guidance literature:
Multi-step reaction with 6 steps
1: 71 percent / pyridinium trifluoroacetate, 1,3-dicyclohexylcarbodiimide / benzene; dimethylsulfoxide / 9 h / Ambient temperature
2: 85 percent / BF3*OEt2 / diethyl ether / 24 h / 25 - 30 °C
3: 95 percent / NaBH4 / methanol; CH2Cl2; CHCl3 / 0.08 h
4: 1.) NaH / 1) THF, 25 min; 2) THF, 50 min
5: 88 percent / Martin's sulfurane / CDCl3 / 0.33 h
6: 84 percent / 4-methylmorpholine-N-oxide, OsO4 / 2-methyl-propan-2-ol; acetone; H2O / 16 h
With sodium tetrahydroborate; osmium(VIII) oxide; Martins sulfurane; boron trifluoride diethyl etherate; pyridinium trifluroacetate; sodium hydride; 4-methylmorpholine N-oxide; dicyclohexyl-carbodiimide; In methanol; diethyl ether; chloroform-d1; dichloromethane; chloroform; water; dimethyl sulfoxide; acetone; tert-butyl alcohol; benzene;
DOI:10.1021/ja971304x
upstream raw materials:

C36H31N3O5

C36H31N3O7

C35H31N3O6

C35H31N3O6

Downstream raw materials:

staurosporine

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