7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

Base Information

Chemical Name:7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one
CAS No.:1323075-36-0
Molecular Formula:C₂₇H₃₁N₅O₄
Molecular Weight:489.574
Hs Code.:

Synonyms:7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

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Chemical Property of 7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

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Technology Process of 7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

There total 8 articles about 7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-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: 1.0%

: 1323075-34-8
7-amino-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 1323075-36-0
7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

Guidance literature:: 7-amino-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one; cyclohexanone; With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane;

With water; sodium hydrogencarbonate; In dichloromethane;

Reference yield:

: 17153-20-7
3-methyl isoxazole-4-carboxylic acid

: 1323075-36-0
7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 0 °C

2: pyridine / 0.75 h / 0 - 20 °C

3: ammonium hydroxide; ferrous(II) sulfate heptahydrate / water; methanol / 0.75 h / 50 °C

4: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane

With pyridine; ferrous(II) sulfate heptahydrate; ammonium hydroxide; oxalyl dichloride; sodium tris(acetoxy)borohydride; acetic acid; N,N-dimethyl-formamide; In methanol; dichloromethane; water;

Reference yield:

: 2632-13-5
2-Bromo-4'-methoxyacetophenone

: 1323075-36-0
7-(cyclohexylamino)-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.08 h / 0 °C

1.2: 1 h / 0 - 20 °C

2.1: 1,4-dioxane / 24 h / 105 °C

3.1: pyridine / 0.75 h / 0 - 20 °C

4.1: ammonium hydroxide; ferrous(II) sulfate heptahydrate / water; methanol / 0.75 h / 50 °C

5.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane

With pyridine; ferrous(II) sulfate heptahydrate; ammonium hydroxide; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;