(R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

Base Information

Chemical Name:(R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol
CAS No.:614761-27-2
Molecular Formula:C₂₃H₂₃FN₂OS
Molecular Weight:394.513
Hs Code.:

Synonyms:(R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

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Chemical Property of (R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

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Technology Process of (R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

There total 1 articles about (R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol 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: 99.0%

: 872-31-1
3-Bromothiophene

: (4aR)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hyxahydro-1H-benzo[f]indazole-5-carbaldehyde

: 614761-27-2
(R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

Guidance literature:: With tert.-butyl lithium; In diethyl ether; at -78 ℃;
DOI:10.1021/jm030585i

Reference yield: 80.0%

: 614761-27-2
(R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

: 614761-78-3
(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanone

Guidance literature:: With N-methyl-2-indolinone; tetrapropylammonium perruthennate; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1021/jm030585i

Reference yield:

: 614761-27-2
(R)-(3-thienyl)[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]methanol

: 1-[1-(4-fluoro-phenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]-1-thiophen-3-yl-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / NMO; TPAP / CH₂Cl₂ / 3 h / 0 °C

2: 42 percent / diethyl ether / 0.75 h / -40 °C

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; In diethyl ether; dichloromethane;
DOI:10.1021/jm030585i