N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

Base Information

Chemical Name:N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide
CAS No.:105695-46-3
Molecular Formula:C₂₁H₂₈N₄O₃
Molecular Weight:384.478
Hs Code.:

Synonyms:N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

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Chemical Property of N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

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Technology Process of N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

There total 5 articles about N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide 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:

: 105728-47-0
N-cyclohexyl-N-methyl-4-<3-(azidomethyl)-4-nitrophenoxy>butyramide

: 105695-46-3
N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / 10percent Pd/C / ethanol / 3102.9 Torr

2: 97 percent / tetrahydrofuran

3: tetrahydrofuran / 3 h / Ambient temperature

4: N,N-diisopropylamine / acetonitrile / 24 h / Heating

With hydrogen; diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1021/jm00385a012

Reference yield:

: Methanesulfonic acid 5-[3-(cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzyl ester

: 105695-46-3
N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

Guidance literature:: Multi-step reaction with 5 steps

1: aq. NaN₃ / tetrahydrofuran / 1 h / 50 °C

2: H₂ / 10percent Pd/C / ethanol / 3102.9 Torr

3: 97 percent / tetrahydrofuran

4: tetrahydrofuran / 3 h / Ambient temperature

5: N,N-diisopropylamine / acetonitrile / 24 h / Heating

With sodium azide; hydrogen; diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1021/jm00385a012

Reference yield:

: 105728-48-1
N-cyclohexyl-N-methyl-4-<(3-hydroxymethyl)-4-nitrophenoxy>butyramide

: 105695-46-3
N-cyclohexyl-N-methyl-4-<(1,2,3,5-tetrahydro-3-oxoimidazo<2,1-b>quinazolin-7-yl)oxy>butyramide

Guidance literature:: Multi-step reaction with 6 steps

1: Et₃N / tetrahydrofuran

2: aq. NaN₃ / tetrahydrofuran / 1 h / 50 °C

3: H₂ / 10percent Pd/C / ethanol / 3102.9 Torr

4: 97 percent / tetrahydrofuran

5: tetrahydrofuran / 3 h / Ambient temperature

6: N,N-diisopropylamine / acetonitrile / 24 h / Heating

With sodium azide; hydrogen; triethylamine; diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1021/jm00385a012