N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

Base Information

Chemical Name:N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide
CAS No.:853018-90-3
Molecular Formula:C₂₆H₃₄N₄O₄S
Molecular Weight:498.646
Hs Code.:

Synonyms:N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

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Chemical Property of N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

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Technology Process of N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

There total 4 articles about N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide 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:

: 853020-22-1
2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2(3H)-yl] ethanamine

: 124-63-0
methanesulfonyl chloride

: 853018-90-3
N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 75 ℃; for 16h;

Reference yield:

: 66-83-1
5-methoxytryptamine hydrochloride

: 853018-90-3
N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetic acid / 1 h / 100 °C

1.2: 72 h

2.1: potassium carbonate / methanol; acetonitrile / 2 h / 70 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 100 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / Heating / reflux

5.1: potassium carbonate / acetonitrile / 16 h / 75 °C

With lithium aluminium tetrahydride; potassium carbonate; acetic acid; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 853020-88-9,853020-89-0,853020-91-4
1'-benzyl-6-methoxy-2,3,4,9-tetrahydrospiro[β-carboline-1,3'-pyrrolidine]

: 853018-90-3
N-{2-[6-methoxy-1'-(2-phenoxyethyl)-4,9-dihydrospiro[β-carboline-1,3'-pyrrolidin]-2 (3H)-yl]ethyl}methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen / palladium dihydroxide / methanol; water / 58 °C

2: potassium carbonate / methanol; acetonitrile / 2 h / 70 °C

3: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 100 °C

4: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / Heating / reflux

5: potassium carbonate / acetonitrile / 16 h / 75 °C

With lithium aluminium tetrahydride; hydrogen; potassium carbonate; palladium dihydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile;