trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Base Information

Chemical Name:trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide
CAS No.:951656-02-3
Molecular Formula:C₂₄H₂₄N₂O₅
Molecular Weight:420.465
Hs Code.:

Synonyms:trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Suppliers and Price of trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

There total 8 articles about trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide 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: 43.0%

: 951655-98-4
trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]acrylic acid

: 6723-30-4
O-2-tetrahydro-2H-pyranhydroxylamine

: 951656-02-3
trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1021/jm0703136

Reference yield:

: 951655-88-2
(1-benzenesulfonyl-5-[1,3]dioxolan-2-yl-1H-indol-2-yl)-(3-methoxyphenyl)methanone

: 951656-02-3
trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: 31 percent / aq. HClO₄ / CH₂Cl₂ / 0 °C

2: 73 percent / aq. NaOH; NEt₃ / CH₂Cl₂ / 1 h / 20 °C

3: 47 percent / TFA / 1 h / 20 °C

4: 24 percent / aq. NaOH / methanol / 12 h / Heating

5: 43 percent / BOP; NEt₃ / dimethylformamide / 1 h / 20 °C

With sodium hydroxide; perchloric acid; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide; 2: Wittig olefination;
DOI:10.1021/jm0703136

Reference yield:

: 951655-90-6
1-benzenesulfonyl-2-(3-methoxybenzoyl)-1H-indole-5-carbaldehyde

: 951656-02-3
trans-3-[2-(3-methoxybenzoyl)-1H-indol-5-yl]-N-(tetrahydropyran-2-yloxy)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / aq. NaOH; NEt₃ / CH₂Cl₂ / 1 h / 20 °C

2: 47 percent / TFA / 1 h / 20 °C

3: 24 percent / aq. NaOH / methanol / 12 h / Heating

4: 43 percent / BOP; NEt₃ / dimethylformamide / 1 h / 20 °C

With sodium hydroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: Wittig olefination;
DOI:10.1021/jm0703136