1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

Base Information

Chemical Name:1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one
CAS No.:1325189-12-5
Molecular Formula:C₁₉H₃₀N₄O₂
Molecular Weight:346.473
Hs Code.:

Synonyms:1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

Suppliers and Price of 1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

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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 1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

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Technology Process of 1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

There total 5 articles about 1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one 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: 55.0%

: 1325189-94-3
C₁₄H₂₁N₃O₂

: 55-86-7
mechlorethamine hydrochloride

: 1325189-12-5
1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; for 16h; Reflux;

Reference yield: 55.0%

: 1325189-94-3
C₁₄H₂₁N₃O₂

: 51-75-2
nitrogen mustard

: 1325189-12-5
1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; for 16h; Reflux;

Reference yield:

: 1325189-91-0
C₁₄H₁₉N₃O₄

: 1325189-12-5
1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium on activated charcoal / methanol

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / Reflux

With hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; acetonitrile;