6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

Base Information

Chemical Name:6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole
CAS No.:134274-08-1
Molecular Formula:C₁₉H₂₂N₂O₂
Molecular Weight:310.396
Hs Code.:

Synonyms:6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

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Chemical Property of 6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

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Technology Process of 6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

There total 4 articles about 6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-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: 80.0%

: 134274-04-7
6,7-methylenedioxy-9-(N-4-methylcyclohexyliminio)-9H-pyrrolo<1.2-a>indole hydrobromide

: 134274-08-1
6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

Guidance literature:: With sodium tetrahydroborate; In methanol; for 1h; Heating;

Reference yield:

: 134273-67-9
2-(1-pyrrolyl)piperonylic acid

: 134274-08-1
6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

Guidance literature:: Multi-step reaction with 4 steps

1: PCl₅ / benzene

3: 1) Na₂CO₃, 2) 40percent HBr / 1) DMF, 2h, reflux, 2) EtOH, HOAc, RT, 30 min

4: 80 percent / NaBH₄ / methanol / 1 h / Heating

With sodium tetrahydroborate; phosphorus pentachloride; hydrogen bromide; sodium carbonate; In methanol; benzene;

Reference yield:

: 134273-68-0
2-(1-pyrrolyl)piperonyl chlorid

: 134274-08-1
6,7-methylenedioxy-9-N-(4-methylcyclohexylamino)-9H-pyrrolo<1.2-a>indole

Guidance literature:: Multi-step reaction with 3 steps

2: 1) Na₂CO₃, 2) 40percent HBr / 1) DMF, 2h, reflux, 2) EtOH, HOAc, RT, 30 min

3: 80 percent / NaBH₄ / methanol / 1 h / Heating

With sodium tetrahydroborate; hydrogen bromide; sodium carbonate; In methanol;