tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

Base Information

Chemical Name:tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate
CAS No.:1138038-85-3
Molecular Formula:C₂₂H₂₅ClN₄O₅S
Molecular Weight:492.983
Hs Code.:

Synonyms:tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

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Chemical Property of tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

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Technology Process of tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

There total 1 articles about tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate 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: 98.0%

: 1138038-78-4
tert-butyl ({1-(2-chlorophenyl)-5-[(6-chloropyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

: 124-41-4
sodium methylate

: 1138038-85-3
tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

Guidance literature:: In methanol; at 20 ℃; for 1h;

Reference yield:

: 1138038-85-3
tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate

: 1138043-15-8
1-{1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}-N-methylmethanamine

Guidance literature:: tert-butyl ({1-(2-chlorophenyl)-5-[(6-methoxypyridin-3-yl)sulfonyl]-1H-pyrazol-3-yl}methyl)methylcarbamate; With hydrogenchloride; In ethyl acetate; isopropyl alcohol; at 20 ℃; for 4h;

With sodium hydrogencarbonate; In water;