6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

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Chemical Name:6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one
CAS No.:184763-58-4
Molecular Formula:C₁₆H₂₄N₄O
Molecular Weight:288.393
Hs Code.:

Synonyms:6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

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Chemical Property of 6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

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Technology Process of 6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

There total 3 articles about 6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-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: 75.7%

: 184766-43-6
(1,1-Dimethyl-2-{methyl-[4-(4-methyl-6-oxo-1,4,5,6-tetrahydro-pyridazin-3-yl)-phenyl]-amino}-ethyl)-carbamic acid tert-butyl ester

: 184763-58-4
6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

Guidance literature:: With hydrogenchloride; ethyl acetate; for 0.5h; Ambient temperature;
DOI:10.1248/cpb.44.2061

Reference yield:

: 184766-30-1
4-[4-(2-tert-Butoxycarbonylamino-2-methyl-propylamino)-phenyl]-3-methyl-4-oxo-butyric acid methyl ester

: 184763-58-4
6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 3 steps

1: 64.9 percent / NaBH₃CN, AcOH / methanol / 10 h / Heating

2: 88 percent / hydrazine hydrate / ethanol / 3 h / Heating

3: 75.7 percent / 2.3N HCl/AcOEt / 0.5 h / Ambient temperature

With hydrogenchloride; sodium cyanoborohydride; hydrazine hydrate; acetic acid; ethyl acetate; In methanol; ethanol;
DOI:10.1248/cpb.44.2061

Reference yield:

: 184766-37-8
4-{4-[(2-tert-Butoxycarbonylamino-2-methyl-propyl)-methyl-amino]-phenyl}-3-methyl-4-oxo-butyric acid methyl ester

: 184763-58-4
6-{4-[(2-Amino-2-methyl-propyl)-methyl-amino]-phenyl}-5-methyl-4,5-dihydro-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / hydrazine hydrate / ethanol / 3 h / Heating

2: 75.7 percent / 2.3N HCl/AcOEt / 0.5 h / Ambient temperature

With hydrogenchloride; hydrazine hydrate; ethyl acetate; In ethanol;
DOI:10.1248/cpb.44.2061