1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

Base Information

Chemical Name:1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one
CAS No.:98754-18-8
Molecular Formula:C₂₁H₂₂ClN₃O₂
Molecular Weight:383.878
Hs Code.:

Synonyms:1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

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Chemical Property of 1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

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Technology Process of 1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

There total 6 articles about 1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-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: 83.4%

: 1-Piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-one; hydrochloride

: 536-38-9
4-chlorobenzoylmethyl bromide

: 98754-18-8
1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

Guidance literature:: With TEA; In N,N-dimethyl-formamide; Ambient temperature;
DOI:10.1248/cpb.33.1116

Reference yield:

: 3612-20-2
1-phenylmethyl-4-piperidone

: 98754-18-8
1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 56.9 percent / p-toluenesulfonic acid monohydrate / benzene / 6 h / Heating

2: 51.6 percent / LiAlH₄ / dioxane / 6 h / Heating

3: 48.6 percent / acetonitrile / 3 h / 40 - 60 °C

4: 44.2 percent / hydrogen, 1 N aq.HCl / 10percent Pd-C / H₂O; methanol / 5 h / 40 °C

5: 83.4 percent / TEA / dimethylformamide / Ambient temperature

With hydrogenchloride; lithium aluminium tetrahydride; TEA; hydrogen; toluene-4-sulfonic acid; palladium on activated charcoal; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1248/cpb.33.1116

Reference yield:

: 28144-70-9,88-68-6
anthranilic acid amide

: 98754-18-8
1-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-1H-quinazolin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 56.9 percent / p-toluenesulfonic acid monohydrate / benzene / 6 h / Heating

2: 51.6 percent / LiAlH₄ / dioxane / 6 h / Heating

3: 48.6 percent / acetonitrile / 3 h / 40 - 60 °C

4: 44.2 percent / hydrogen, 1 N aq.HCl / 10percent Pd-C / H₂O; methanol / 5 h / 40 °C

5: 83.4 percent / TEA / dimethylformamide / Ambient temperature

With hydrogenchloride; lithium aluminium tetrahydride; TEA; hydrogen; toluene-4-sulfonic acid; palladium on activated charcoal; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1248/cpb.33.1116