(+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

Base Information

Chemical Name:(+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole
CAS No.:324079-73-4
Molecular Formula:C₂₆H₂₄N₂O
Molecular Weight:380.489
Hs Code.:

Synonyms:(+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

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Chemical Property of (+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

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Technology Process of (+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

There total 5 articles about (+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole 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: 29.0%

: 2912-98-3
(R)-1-Phenylethylhydroxylamine

: (E)-1-cinnamylindole-2-carbaldehyde

: (+)-(αR,1S,4R,12S)-2-(α-phenylethyl)-12-phenyl-1,2,4,5-tetrahydro-1,4-methanoindolo[2,1-d][1,2,5]oxadiazepine

: (-)-(αR,1R,4S,12R)-2-(α-phenylethyl)-12-phenyl-1,2,4,5-tetrahydro-1,4-methanoindolo[2,1-d][1,2,5]oxadiazepine

: 324079-73-4
(+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

: 324079-74-5
(+)-(αR,3R,3aR,10bR)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

Guidance literature:: With aluminum oxide; In toluene; for 120h; Heating;
DOI:10.1021/jo000842g

Reference yield:

: 3770-50-1,117770-52-2
2-carbethoxyindole

: 324079-73-4
(+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

Guidance literature:: Multi-step reaction with 4 steps

1: 48 percent / NaOH; TEBA / benzene; H₂O / 1 h / 20 °C

2: 78 percent / LiAlH₄ / tetrahydrofuran / 2 h / 20 °C

3: 52 percent / MnO₂ / CH₂Cl₂ / 12 h / 20 °C

4: 29 percent / Al₂O₃ / toluene / 120 h / Heating

With manganese(IV) oxide; aluminum oxide; sodium hydroxide; lithium aluminium tetrahydride; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran; dichloromethane; water; toluene; benzene;
DOI:10.1021/jo000842g

Reference yield:

: 4392-24-9
Cinnamyl bromide

: 324079-73-4
(+)-(αR,3S,3aS,10bS)-1-(α-phenylethyl)-3-phenyl-1,3a,4,10b-tetrahydro-3H-isoxazolo[3',4':3,4]pyrrolo[1,2-a]indole

Guidance literature:: Multi-step reaction with 4 steps

1: 48 percent / NaOH; TEBA / benzene; H₂O / 1 h / 20 °C

2: 78 percent / LiAlH₄ / tetrahydrofuran / 2 h / 20 °C

3: 52 percent / MnO₂ / CH₂Cl₂ / 12 h / 20 °C

4: 29 percent / Al₂O₃ / toluene / 120 h / Heating

With manganese(IV) oxide; aluminum oxide; sodium hydroxide; lithium aluminium tetrahydride; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran; dichloromethane; water; toluene; benzene;
DOI:10.1021/jo000842g