ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

Base Information

Chemical Name:ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate
CAS No.:138129-20-1
Molecular Formula:C₂₁H₁₈F₃N₃O₄
Molecular Weight:433.387
Hs Code.:

Synonyms:ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

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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 ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

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Technology Process of ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

There total 1 articles about ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate 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:

: 351-38-2
N-chloroacetyl-3-(trifluoromethyl)aniline

: 25947-13-1
ethyl 1,2-dihydro-1-oxophthalazin-4-ylacetate

: 138129-20-1
ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

Guidance literature:: With potassium tert-butylate; Yield given. Multistep reaction; 1.) DMF, RT, 30 min, 2.) DMF, RT, 30 min;
DOI:10.1021/jm00081a006

Reference yield: 45.0%

: 138129-20-1
ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

: 138129-27-8
ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-thioxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

Guidance literature:: With tetraphosphorus decasulfide; In benzene; at 70 ℃; for 3h;
DOI:10.1021/jm00081a006

Reference yield:

: 138129-20-1
ethyl 3-<2-<<3-(trifluoromethyl)phenyl>amino>-2-oxoethyl>-3,4-dihydro-4-oxo-1-phthalazineacetate

: 138129-43-8
{4-Oxo-3-[(3-trifluoromethyl-phenylthiocarbamoyl)-methyl]-3,4-dihydro-phthalazin-1-yl}-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / P₂S₅ / benzene / 3 h / 70 °C

2: aq. KOH

With potassium hydroxide; tetraphosphorus decasulfide; In benzene;
DOI:10.1021/jm00081a006