(3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

Base Information

Chemical Name:(3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide
CAS No.:134931-33-2
Molecular Formula:C₂₂H₂₆N₂O₂
Molecular Weight:350.461
Hs Code.:

Synonyms:(3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

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Chemical Property of (3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

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Technology Process of (3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

There total 5 articles about (3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide 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:

: 39160-50-4
5-Methoxy-3a-methyl-1,3,3a,8a-tetrahydro-indeno[2,1-b]pyrrole-2,8-dione

: 134931-33-2
(3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

Guidance literature:: Multi-step reaction with 4 steps

1: H₂, HCl(gas) / 10percent Pd/C / acetic acid / 4 h / 70 °C / 2844.3 Torr

2: 90 percent / LiAlH₄ / tetrahydrofuran / 5 h / Heating

4: CH₂Cl₂

With hydrogenchloride; lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetic acid;
DOI:10.1021/jm00086a011

Reference yield:

: 39160-49-1
{2-[(E)-Hydroxyimino]-6-methoxy-1-methyl-3-oxo-indan-1-yl}-acetic acid methyl ester

: 134931-33-2
(3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / H₂, HCl(gas) / 10percent Pd/C / acetic acid / 4 h / 2585.7 Torr / Heating

2: H₂, HCl(gas) / 10percent Pd/C / acetic acid / 4 h / 70 °C / 2844.3 Torr

3: 90 percent / LiAlH₄ / tetrahydrofuran / 5 h / Heating

5: CH₂Cl₂

With hydrogenchloride; lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetic acid;
DOI:10.1021/jm00086a011

Reference yield:

: 39160-52-6
3,3a,8,8a-tetrahydro-5-methoxy-3a-methylindeno<2,1-b>pyrrol-2(1H)-one

: 134931-33-2
(3aR,8aS)-5-Methoxy-3a-methyl-3,3a,8,8a-tetrahydro-2H-indeno[2,1-b]pyrrole-1-carboxylic acid ((S)-1-phenyl-ethyl)-amide

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / LiAlH₄ / tetrahydrofuran / 5 h / Heating

3: CH₂Cl₂

With lithium aluminium tetrahydride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00086a011