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

Base Information

Chemical Name:diethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-2,7-dicarboxylate
CAS No.:462117-40-4
Molecular Formula:C₃₀H₃₆N₂O₇
Molecular Weight:536.625
Hs Code.:

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

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

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

There total 3 articles about diethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-2,7-dicarboxylate 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: 76.0%

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

: 462117-26-6
diethyl 4-benzyl-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-2,7-dicarboxylate

: 462117-40-4
diethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-2,7-dicarboxylate

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:

: 391873-71-5
ethyl 4-benzyl-7-formyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate

: 462117-40-4
diethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-2,7-dicarboxylate

Guidance literature:: Multi-step reaction with 3 steps

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

2: xylene / Heating

3: 76 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:

: 7-(2-azido-2-ethoxycarbonyl-vinyl)-4-benzyl-3,4-dihydro-2H-benzo[1,4]oxazine-2-carboxylic acid ethyl ester

: 462117-40-4
diethyl 4-benzyl-6-[2-(tert-butoxycarbonyl)ethyl]-2,3,4,6-tetrahydro[1,4]oxazino[2,3-f]indole-2,7-dicarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: xylene / Heating

2: 76 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