4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

Base Information

Chemical Name:4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate
CAS No.:1393714-29-8
Molecular Formula:C₂₀H₂₃N₃O₃
Molecular Weight:353.421
Hs Code.:

Synonyms:4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

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Chemical Property of 4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

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Technology Process of 4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

There total 4 articles about 4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate 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: 83.0%

: 1393714-27-6
1,2,3,3a,4,9-hexahydro-4-methylpyrrolo[2,1-b]quinazolin-7-ol

: 18908-07-1
3-methoxyphenyl isocyanate

: 1393714-29-8
4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

Guidance literature:: 1,2,3,3a,4,9-hexahydro-4-methylpyrrolo[2,1-b]quinazolin-7-ol; With triethylamine; In dichloromethane; at 20 ℃; for 0.25h;

3-methoxyphenyl isocyanate; In dichloromethane; at 20 ℃;
DOI:10.1021/ml3001825

Reference yield:

: 195986-91-5
6-hydroxy-1,2-dihydro-4H-3,1-benzoxazin-2,4-dione

: 1393714-29-8
4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1 h / 130 °C / 2585.81 - 5171.62 Torr / Sealed tube

2.1: potassium carbonate / N,N-dimethyl-formamide; acetone / 36 h / 20 - 70 °C

3.1: 1,4-dioxane / 90 °C / Sealed tube

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 70 °C / Inert atmosphere

5.1: palladium 10% on activated carbon; hydrogen / ethanol / 24 h / 20 °C

6.1: triethylamine / dichloromethane / 0.25 h / 20 °C

6.2: 20 °C

With lithium aluminium tetrahydride; palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ml3001825

Reference yield:

: 1393714-39-0
7-(benzyloxy)-1,2,3,3a,4,9-hexahydro-4-methylpyrrolo[2,1-b]quinazoline

: 1393714-29-8
4-methyl-1,2,3,3a,4,9-hexahydropyrrolo[2,1-b]quinazolin-7-yl (3-methoxyphenyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: palladium 10% on activated carbon; hydrogen / ethanol / 24 h / 20 °C

2.1: triethylamine / dichloromethane / 0.25 h / 20 °C

2.2: 20 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In ethanol; dichloromethane;
DOI:10.1021/ml3001825