4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

Base Information

Chemical Name:4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine
CAS No.:212578-78-4
Molecular Formula:C₃₃H₄₀N₂O₆
Molecular Weight:560.69
Hs Code.:

Synonyms:4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

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Chemical Property of 4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

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Technology Process of 4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

There total 9 articles about 4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine 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: 70.0%

: 98-88-4
benzoyl chloride

: 212578-77-3
3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

: 212578-78-4
4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;
DOI:10.1021/jm970795t

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 212578-78-4
4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / CH₂Cl₂ / 3 h / 0 °C

2: 94 percent / H₂ / 10percent Pd/C / acetic acid

3: 70 percent / Et₃N / CH₂Cl₂ / 2 h / 0 - 20 °C

With hydrogen; triethylamine; palladium on activated charcoal; In dichloromethane; acetic acid;
DOI:10.1021/jm970795t

Reference yield:

: 120-20-7
2-(3,4-dimethoxyphenyl)-ethylamine

: 212578-78-4
4-benzoyl-3,4-dihydro-2-(3-{[2-(3,4-dimethoxyphenyl)ethyl]-N-(tert-butoxycarbonyl)amino}propyl)-2H-1,4-benzoxazine

Guidance literature:: Multi-step reaction with 5 steps

1: 83 percent / EDCI / CH₂Cl₂ / 5 h / Ambient temperature

2: 81 percent / BH₃*Me₂S / tetrahydrofuran / 4 h / Heating

3: 98 percent / CH₂Cl₂ / 3 h / 0 °C

4: 94 percent / H₂ / 10percent Pd/C / acetic acid

5: 70 percent / Et₃N / CH₂Cl₂ / 2 h / 0 - 20 °C

With dimethylsulfide borane complex; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetic acid;
DOI:10.1021/jm970795t