{4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

Base Information

Chemical Name:{4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone
CAS No.:1357183-48-2
Molecular Formula:C₂₁H₂₃ClN₄O₂
Molecular Weight:398.892
Hs Code.:

Synonyms:{4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

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Chemical Property of {4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

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Technology Process of {4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

There total 5 articles about {4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone 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:

: 110-91-8,99108-56-2
morpholine

: 1357186-05-0
4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazine-1-carboxylic acid

: 1357183-48-2
{4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; at 100 ℃; for 16h; Inert atmosphere;

Reference yield:

: 1357186-03-8
4-chloro-5,6,7,8-tetrahydro-5,8-ethanophthalazine-1-carbonitrile

: 1357183-48-2
{4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride / 1,4-dioxane / 1 h / 150 °C / Microwave irradiation

2.1: sodium hydroxide; water / 8 h / Reflux

2.2: pH 2

3.1: N-ethyl-N,N-diisopropylamine; HATU / 16 h / 100 °C / Inert atmosphere

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In 1,4-dioxane;

Reference yield:

: 202823-67-4
3,6-dichloro-4,5-diazatricyclo[6.2.2.2,7]dodeca-2⁽⁷⁾,3,5-triene

: 1357183-48-2
{4-[(3-chlorophenyl)amino]-5,6,7,8-tetrahydro-5,8-ethanophthalazin-1-yl}(morpholin-4-yl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen iodide; sodium iodide / 0.67 h / 120 °C / Microwave irradiation

2.1: acetonitrile / 0.67 h / 160 °C / Microwave irradiation

3.1: hydrogenchloride / 1,4-dioxane / 1 h / 150 °C / Microwave irradiation

4.1: sodium hydroxide; water / 8 h / Reflux

4.2: pH 2

5.1: N-ethyl-N,N-diisopropylamine; HATU / 16 h / 100 °C / Inert atmosphere

With hydrogenchloride; water; hydrogen iodide; N-ethyl-N,N-diisopropylamine; HATU; sodium iodide; sodium hydroxide; In 1,4-dioxane; acetonitrile;