(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

Base Information

Chemical Name:(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol
CAS No.:1299446-55-1
Molecular Formula:C₂₆H₃₅FN₂OSi
Molecular Weight:438.661
Hs Code.:

Synonyms:(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

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Chemical Property of (4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

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Technology Process of (4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

There total 2 articles about (4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol 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:

: 614763-02-9
(4αS)-1-(4-fluorophenyl)-4α-methyl-4,4α,6,7-tetrahydrocyclopenta[f]indazol-5(1H)-one

: 1299446-55-1
(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 1.5 h / -78 - 20 °C

2: 2,6-dimethylpyridine / dichloromethane / 1.25 h / 0 - 20 °C

With 2,6-dimethylpyridine; In diethyl ether; dichloromethane;

Reference yield:

: 786707-55-9
C₁₉H₁₉FN₂O₂

: 1299446-55-1
(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride; water / tetrahydrofuran / 3.5 h / 65 °C

2: diethyl ether / 1.5 h / -78 - 20 °C

3: 2,6-dimethylpyridine / dichloromethane / 1.25 h / 0 - 20 °C

With 2,6-dimethylpyridine; hydrogenchloride; water; In tetrahydrofuran; diethyl ether; dichloromethane;

Reference yield:

: 1299446-55-1
(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol

: 1299446-56-2
{(4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-yl}acetaldehyde

Guidance literature:: (4αS,5R)-1-(4-fluorophenyl)-4α-methyl-5-(prop-2-en-1yl)-5-[(triethylsilyl)oxy]-1,4,4α,5,6,7-hexahydrocyclopenta[f]indazol-5-ol; With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; at 20 ℃; for 2h;

With sodium periodate; In methanol; at 20 ℃; for 2h;