methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

Base Information

Chemical Name:methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate
CAS No.:1214271-95-0
Molecular Formula:C₂₆H₂₈F₃N₅O₃
Molecular Weight:527.44
Hs Code.:

Synonyms:methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

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Chemical Property of methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

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Technology Process of methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

There total 6 articles about methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate 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:

: 1214271-94-9
methyl [2-(4-aminobenzyl)-4,6-bis([(2H)6]dimethyl-amino)pyrimidin-5-yl]acetate

: 329-15-7
4-trifluoromethyl-phenyl acetyl chloride

: 1214271-95-0
methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 0.5h;

Reference yield:

: 780763-91-9
[4,6-dihydroxy-2-(4-nitrobenzyl)pyrimidin-5-yl]acetic acid methyl ester

: 1214271-95-0
methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate; N,N-dimethyl-aniline / toluene / 3 h / Reflux

2: N-ethyl-N,N-diisopropylamine; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / 20 - 145 °C

3: hydrogen / palladium 10% on activated carbon / methanol / 3.17 h / 20 °C

4: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; hydrogen; N,N-dimethyl-aniline; triethylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate; palladium 10% on activated carbon; In methanol; dichloromethane; toluene;

Reference yield:

: 555-21-5,34512-13-5,174848-08-9
4-Nitrophenylacetonitrile

: 1214271-95-0
methyl [4,6-bis([(2H)6]dimethylamino)-2-(4-{[4-(trifluoromethyl)benzoyl]amino}benzyl)pyrimidin-5-yl]acetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogenchloride / 1,4-dioxane; ethanol / 22 h / 20 °C

1.2: 3 h

2.1: sodium methylate / methanol / 3 h / Reflux

2.2: 0 °C

3.1: trichlorophosphate; N,N-dimethyl-aniline / toluene / 3 h / Reflux

4.1: N-ethyl-N,N-diisopropylamine; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / 20 - 145 °C

5.1: hydrogen / palladium 10% on activated carbon / methanol / 3.17 h / 20 °C

6.1: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

With hydrogenchloride; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; hydrogen; sodium methylate; N,N-dimethyl-aniline; triethylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate; palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethanol; dichloromethane; toluene;