(1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

Base Information

Chemical Name:(1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester
CAS No.:1418200-16-4
Molecular Formula:C₂₃H₂₄N₄O₅S
Molecular Weight:468.533
Hs Code.:

Synonyms:(1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

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Chemical Property of (1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

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Technology Process of (1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

There total 5 articles about (1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester 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: 93.0%

: 598-81-2
(R)-lactamide

: 1418200-15-3
(1S,3R)-3-(5-amino-1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-4-ylamino)-cyclopentanecarboxylic acid methyl ester

: 1418200-16-4
(1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

Guidance literature:: (R)-lactamide; With triethyloxonium fluoroborate; In tetrahydrofuran; at 20 ℃; for 1h;

(1S,3R)-3-(5-amino-1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-4-ylamino)-cyclopentanecarboxylic acid methyl ester; In tetrahydrofuran; ethanol; at 90 ℃; for 3h;

Reference yield:

: 1418200-14-2
(1S,3R)-3-(1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-ylamino)-cyclopentanecarboxylic acid methyl ester

: 1418200-16-4
(1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C

2.1: triethyloxonium fluoroborate / tetrahydrofuran / 1 h / 20 °C

2.2: 3 h / 90 °C

With palladium 10% on activated carbon; hydrogen; triethyloxonium fluoroborate; In tetrahydrofuran; ethanol;

Reference yield:

: 1418200-13-1
(1S,3R)-3-(1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-ylamino)-cyclopentanecarboxylic acid

: 1418200-16-4
(1S,3R)-3-[6-benzenesulfonyl-2-((R)-1-hydroxyethyl)-6H-1,3,5,6-tetraaza-as-indacen-1-yl]-cyclopentanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / 1 h / 60 °C

2.1: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C

3.1: triethyloxonium fluoroborate / tetrahydrofuran / 1 h / 20 °C

3.2: 3 h / 90 °C

With thionyl chloride; palladium 10% on activated carbon; hydrogen; triethyloxonium fluoroborate; In tetrahydrofuran; ethanol;