ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

Base Information

Chemical Name:ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate
CAS No.:462117-41-5
Molecular Formula:C₃₁H₃₈N₂O₇
Molecular Weight:550.652
Hs Code.:

Synonyms:ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

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Chemical Property of ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

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Technology Process of ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

There total 3 articles about ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate 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: 94.0%

: 1663-39-4,25232-27-3
tert-Butyl acrylate

: 462117-27-7
ethyl 4-benzyl-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

: 462117-41-5
ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

Guidance literature:: With N-benzyl-trimethylammonium hydroxide; In water; N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1002/1099-0690(200205)2002:10<1646::AID-EJOC1646>3.0.CO;2-K

Reference yield:

: ethyl 4-benzyl-7-formyl-2,3-dihydro-1,4-benzoxazine-2-acetate

: 462117-41-5
ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium ethoxide / ethanol / 20 h / -18 °C

2: xylene / Heating

3: 94 percent / Triton B / dimethylformamide; H₂O / 4 h / 20 °C

With sodium ethanolate; N-benzyl-trimethylammonium hydroxide; In ethanol; water; N,N-dimethyl-formamide; xylene; 1: Hemetsberger reaction / 2: Hemetsberger reaction;
DOI:10.1002/1099-0690(200205)2002:10<1646::AID-EJOC1646>3.0.CO;2-K

Reference yield:

: 2-azido-3-(4-benzyl-2-ethoxycarbonylmethyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-acrylic acid ethyl ester

: 462117-41-5
ethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2-[(ethoxycarbonyl)methyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-7-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: xylene / Heating

2: 94 percent / Triton B / dimethylformamide; H₂O / 4 h / 20 °C

With N-benzyl-trimethylammonium hydroxide; In water; N,N-dimethyl-formamide; xylene; 1: Hemetsberger reaction;
DOI:10.1002/1099-0690(200205)2002:10<1646::AID-EJOC1646>3.0.CO;2-K