Technology Process of C33H33NO4*ClH
There total 6 articles about C33H33NO4*ClH which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
formic acid; C32H33NO4*ClH;
With
acetic acid;
In
water;
at 90 ℃;
With
hydrogenchloride;
In
methanol;
at -20 ℃;
DOI:10.1016/j.bmcl.2012.01.005
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 180 °C / Neat (no solvent)
2.1: trichlorophosphate / benzene / 80 °C
3.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide
4.1: hydrogenchloride / methanol; diethyl ether / -20 °C
5.1: acetic acid / water / 90 °C
5.2: -20 °C
With
hydrogenchloride; formic acid; [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; acetic acid; triethylamine; trichlorophosphate;
In
methanol; diethyl ether; water; N,N-dimethyl-formamide; benzene;
2.1: Bischler-Napieralski reaction / 5.1: Mannich reaction;
DOI:10.1016/j.bmcl.2012.01.005
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: trichlorophosphate / benzene / 80 °C
2.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide
3.1: hydrogenchloride / methanol; diethyl ether / -20 °C
4.1: acetic acid / water / 90 °C
4.2: -20 °C
With
hydrogenchloride; formic acid; [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; acetic acid; triethylamine; trichlorophosphate;
In
methanol; diethyl ether; water; N,N-dimethyl-formamide; benzene;
1.1: Bischler-Napieralski reaction / 4.1: Mannich reaction;
DOI:10.1016/j.bmcl.2012.01.005