(2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

Base Information

Chemical Name:(2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide
CAS No.:235423-16-2
Molecular Formula:C₁₅H₁₄N₂O₄S
Molecular Weight:318.353
Hs Code.:

Synonyms:(2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

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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 (2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

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Technology Process of (2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

There total 5 articles about (2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide 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:

: 204690-21-1
(Z)-(5-ethoxycarbonylmethyl-4-oxothiazolidin-2-ylidene)-N-phenylethanamide

: 235423-16-2
(2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

: 235423-20-8
(2E,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

Guidance literature:: (Z)-(5-ethoxycarbonylmethyl-4-oxothiazolidin-2-ylidene)-N-phenylethanamide; With bromine; In chloroform; at 0 ℃;

at 20 ℃; for 5h; Title compound not separated from byproducts; evacuation;
DOI:10.1016/S0040-4020(01)00496-3

Reference yield:

: 204690-21-1
(Z)-(5-ethoxycarbonylmethyl-4-oxothiazolidin-2-ylidene)-N-phenylethanamide

: 235423-16-2
(2Z,5Z)-N-phenyl (5-ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)ethanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: PHBP / acetonitrile / 0.5 h / 0 °C

1.2: acetonitrile / 80 - 85 °C

2.1: dimethylsulfoxide-d6

With PHBP; In dimethylsulfoxide-d6; acetonitrile;
DOI:10.3987/COM-03-9980