methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

Base Information

Chemical Name:methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate
CAS No.:780763-94-2
Molecular Formula:C₁₆H₁₉ClN₄O₂
Molecular Weight:334.805
Hs Code.:

Synonyms:methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

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Chemical Property of methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

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Technology Process of methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

There total 5 articles about methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]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: 95.0%

: 780763-93-1
methyl [4-chloro-6-(dimethylamino)-2-(4-nitrobenzyl)-5-pyrimidinyl]acetate

: 780763-94-2
methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

Guidance literature:: palladium 10% on activated carbon; In anhydrous THF; for 13h;

Reference yield:

: 780763-92-0
[4,6-dichloro-2-(4-nitrobenzyl)pyrimidin-5-yl]acetic acid methyl ester

: 780763-94-2
methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: N,N-dimethylammonium chloride; N-ethyl-N,N-diisopropylamine / anhydrous DMF / 16 h / 85 °C

2: palladium 10% on activated carbon / anhydrous THF / 13 h

With N,N-dimethylammonium chloride; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In anhydrous DMF; anhydrous THF;

Reference yield:

: 39695-96-0
2-(4-nitrophenyl)ethanimidamide hydrochloride

: 780763-94-2
methyl [2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)-5-pyrimidinyl]acetate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium methylate / methanol / 16 h / Heating / reflux

2: N,N-dimethyl-aniline; trichlorophosphate / 16 h / Heating / reflux

3: N,N-dimethylammonium chloride; N-ethyl-N,N-diisopropylamine / anhydrous DMF / 16 h / 85 °C

4: palladium 10% on activated carbon / anhydrous THF / 13 h

With N,N-dimethylammonium chloride; sodium methylate; N,N-dimethyl-aniline; N-ethyl-N,N-diisopropylamine; trichlorophosphate; palladium 10% on activated carbon; In methanol; anhydrous DMF; anhydrous THF;