((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

Base Information

Chemical Name:((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate
CAS No.:1403934-98-4
Molecular Formula:C₃₂H₄₁NO₉Si
Molecular Weight:611.764
Hs Code.:

((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

Synonyms:((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

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Chemical Property of ((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

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Technology Process of ((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

There total 5 articles about ((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate 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: 64.0%

: 1403934-97-3
(3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-11-(hydroxymethyl)-6-methoxy-2,2-dimethyl-3b,4,10b,11,12,12a-hexahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-5(3aH)-one

: 98-88-4
benzoyl chloride

: 1403934-98-4
((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 ℃; Inert atmosphere;
DOI:10.1139/v2012-073

Reference yield:

: 1329120-38-8
{(3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-4-[(4-methylphenyl)sulfonyl]-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl}methyl acetate

: 1403934-98-4
((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: naphthalene; sodium / 1,2-dimethoxyethane / -50 °C / Inert atmosphere

2: triethylamine; dmap / dichloromethane / 0 °C / Inert atmosphere

With dmap; naphthalene; sodium; triethylamine; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1139/v2012-073

Reference yield:

: 1329120-36-6
(3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-11-(hydroxymethyl)-6-methoxy-2,2-dimethyl-4-[(4-methylphenyl)sulfonyl]-3,3b,4,5,10b,11,12,12aoctahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-5-ol

: 1403934-98-4
((3aS,3bR,10bR,11S,12S,12aS)-12-{[tert-butyl(dimethyl)silyl]oxy}-6-methoxy-2,2-dimethyl-5-oxo-3a,3b,4,5,10b,11,12,12a-octahydrobis[1,3]dioxolo[4,5-c:4',5'-j]phenanthridin-11-yl)methyl benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 24 h / Inert atmosphere

2: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / Inert atmosphere; Molecular sieve

3: naphthalene; sodium / 1,2-dimethoxyethane / -50 °C / Inert atmosphere

4: triethylamine; dmap / dichloromethane / 0 °C / Inert atmosphere

With pyridine; dmap; tetrapropylammonium perruthennate; naphthalene; sodium; 4-methylmorpholine N-oxide; triethylamine; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1139/v2012-073