((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

Base Information

Chemical Name:((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol
CAS No.:1418200-18-6
Molecular Formula:C₂₈H₃₈N₄O₄SSi
Molecular Weight:554.786
Hs Code.:

Synonyms:((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

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Chemical Property of ((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

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Technology Process of ((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

There total 7 articles about ((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol 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%

: 1418200-17-5
(1S,3R)-3-(6-benzenesulfonyl-2-(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentanecarboxylic acid methyl ester

: 1418200-18-6
((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

Guidance literature:: With sodium tetrahydroborate; In ethanol; at 20 ℃; for 1h;

Reference yield:

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

: 1418200-18-6
((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

Guidance literature:: Multi-step reaction with 3 steps

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

1.2: 3 h / 90 °C

2.1: 1H-imidazole / dichloromethane / 20 °C

3.1: sodium tetrahydroborate / ethanol / 1 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; triethyloxonium fluoroborate; In tetrahydrofuran; ethanol; dichloromethane;

Reference yield:

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

: 1418200-18-6
((1S,3R)-3-(6-benzenesulfonyl-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-6H-1,3,5,6-tetraaza-as-indacen-1-yl)-cyclopentyl)-methanol

Guidance literature:: Multi-step reaction with 4 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

3.1: 1H-imidazole / dichloromethane / 20 °C

4.1: sodium tetrahydroborate / ethanol / 1 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; triethyloxonium fluoroborate; In tetrahydrofuran; ethanol; dichloromethane;