(S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

Base Information

Chemical Name:(S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate
CAS No.:1185774-43-9
Molecular Formula:C₂₃H₂₆ClN₃O₅
Molecular Weight:459.93
Hs Code.:

Synonyms:(S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

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Technology Process of (S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

There total 2 articles about (S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate 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: 80.0%

: 131609-35-3
3-(4-chlorobenzyl)-1,3-dihydroindol-2-one

: 2446-83-5
di-isopropyl azodicarboxylate

: 1185774-43-9
(S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

Guidance literature:: With 1,4-bis(9-O-dihydroquinidine)phthalazine; In 1,1,2-trichloroethane; at 20 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ol901405r

Reference yield:

: 131609-35-3
3-(4-chlorobenzyl)-1,3-dihydroindol-2-one

: 2446-83-5
di-isopropyl azodicarboxylate

: 1185774-43-9
(S)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

: (R)-diisopropyl 1-(3-(4-chlorobenzyl)-2-oxoindolin-3-yl)hydrazine-1,2-dicarboxylate

Guidance literature:: 3-(4-chlorobenzyl)-1,3-dihydroindol-2-one; With C₃₀H₃₀F₆N₄OS; In 1,2-dichloro-ethane; at 0 ℃; Inert atmosphere; Molecular sieve;

di-isopropyl azodicarboxylate; In 1,2-dichloro-ethane; at 0 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201100379