5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

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Chemical Name:5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester
CAS No.:135145-06-1
Molecular Formula:C₂₇H₃₈N₂O₇
Molecular Weight:502.608
Hs Code.:

5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

Synonyms:5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

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Chemical Property of 5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

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Technology Process of 5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

There total 2 articles about 5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl 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: 54.0%

: 54620-35-8
(E)-4-Ethyliden-3-methyl-5-thioxo-2-pyrrolidinon

: 135145-01-6
tert-Butyl α-(Triphenylphosphoranylidene)-α-(5-(tert-butoxycarbonyl)-4-(2'-(methoxycarbonyl)ethyl)-3-methylpyrrol-2-yl)acetate

: 135145-08-3,135189-61-6
5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-4,5-dihydro-3H-pyrrol-2-ylsulfanyl]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

: 135145-06-1
5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

: 603-35-0
triphenylphosphine

: 3878-45-3
triphenylphosphine sulfide

Guidance literature:: In xylene; for 5h; Mechanism; Heating; other ylide, other thioimides as substrates;
DOI:10.1021/jo00017a017

Reference yield:

: 7633-32-1
tert-butyl glyoxylate

: 135145-06-1
5-{tert-Butoxycarbonyl-[3-eth-(E)-ylidene-4-methyl-5-oxo-pyrrolidin-(2Z)-ylidene]-methyl}-3-(2-methoxycarbonyl-ethyl)-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / ZnCl₂ / CH₂Cl₂ / 24 h / Ambient temperature

2: 1) N-chlorosuccinimide, dimethyl sulfide / 1) CH₂Cl₂, 5 deg C, 6 h, 2) CH₂Cl₂, room temp., 24h

3: Na₂CO₃

4: 38 percent / xylene / 5 h / Heating

With N-chloro-succinimide; dimethylsulfide; sodium carbonate; zinc(II) chloride; In dichloromethane; xylene;
DOI:10.1021/jo00017a017