4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

Base Information

Chemical Name:4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole
CAS No.:1443332-98-6
Molecular Formula:C₂₄H₂₇ClN₂O₅
Molecular Weight:458.942
Hs Code.:

Synonyms:4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

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Chemical Property of 4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

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Technology Process of 4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

There total 9 articles about 4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-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: 31.0%

: C₂₄H₂₅ClN₂O₅

: 1443332-98-6
4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol; water; at 0 - 20 ℃; for 1h; pH=1 - 3;

Reference yield: 31.0%

: (2R,3R,4S,5S,6R)-2-[4-chloro-3-(4-cyclopropylbenzyl)-1H-indol-1-yl]-6-[(hydroxyimino)methyl]-tetrahydro-2H-pyran-3,4,5-triol

: 1443332-98-6
4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol; water; at 0 - 20 ℃; for 1h;
DOI:10.1016/j.bioorg.2018.11.006

Reference yield:

: 1443332-82-8
C₃₀H₃₀ClNO₈

: 1443332-98-6
4-chloro-3-(4-cyclopropylbenzyl)-1-[6-deoxy-6-(hydroxyamino)-β-D-glucopyranosyl]-1H-indole

Guidance literature:: Multi-step reaction with 3 steps

1: hydroxylamine hydrochloride / pyridine / 2 h / 20 °C

2: sodium methylate / dichloromethane; methanol / 2 h / 0 - 20 °C / Inert atmosphere

3: sodium cyanoborohydride; hydrogenchloride / methanol; water / 1 h / 0 - 20 °C / pH 1 - 3

With hydrogenchloride; hydroxylamine hydrochloride; sodium methylate; sodium cyanoborohydride; In pyridine; methanol; dichloromethane; water;