8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

Base Information

Chemical Name:8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide
CAS No.:268741-84-0
Molecular Formula:C₁₈H₂₃NO₄
Molecular Weight:317.385
Hs Code.:

8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[<i>b</i>]oxepine-7-carboxylic acid amide

Synonyms:8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

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Chemical Property of 8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

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Technology Process of 8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

There total 4 articles about 8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide 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:

: 268741-83-9
4-(4-carbamoyl-3-cyclohexylmethoxy-phenoxy)-butyric acid

: 268741-84-0
8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

Guidance literature:: With PPA; at 80 ℃;
DOI:10.1021/jm0003337

Reference yield:

: 3147-45-3
2,4-dihydroxybenzamide

: 268741-84-0
8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

Guidance literature:: Multi-step reaction with 4 steps

1: Cs₂CO₃ / dimethylformamide

2: Cs₂CO₃ / dimethylformamide

3: LiOH / tetrahydrofuran

4: PPA / 80 °C

With lithium hydroxide; caesium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Alkylation / 2: Alkylation / 3: Hydrolysis / 4: Cyclization;
DOI:10.1021/jm0003337

Reference yield:

: 268741-81-7
4-(4-carbamoyl-3-hydroxy-phenoxy)-butyric acid ethyl ester

: 268741-84-0
8-cyclohexylmethoxy-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-7-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: Cs₂CO₃ / dimethylformamide

2: LiOH / tetrahydrofuran

3: PPA / 80 °C

With lithium hydroxide; caesium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Alkylation / 2: Hydrolysis / 3: Cyclization;
DOI:10.1021/jm0003337