[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

Base Information

Chemical Name:[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester
CAS No.:368426-47-5
Molecular Formula:C₂₇H₂₆N₂O₆S
Molecular Weight:506.579
Hs Code.:

[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[<i>b</i>]azepin-1-yl]-acetic acid benzyl ester

Synonyms:[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

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Chemical Property of [3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

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Technology Process of [3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

There total 9 articles about [3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester 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: 57.0%

: 115010-11-2
2,3-dihydrobenzofuran-5-sulfonyl chloride

: 183508-58-9,103412-68-6
benzyl (3S)-3-amino-2,3,4,5-tetrahydro-2-oxo-1H-benzazepine-1-acetate

: 368426-47-5
[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

Guidance literature:: With 4-methyl-morpholine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/S0960-894X(02)00010-0

Reference yield:

: 4424-80-0
2,3,4,5-tetrahydro-1H-1-benzo[b]azepin-2-one

: 368426-47-5
[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: TMEDA; NaI / acetonitrile / -5 °C

2.1: 95 percent / I₂ / -5 - 20 °C

3.1: NH₃ / aq. ethanol / 0 - 20 °C

3.2: L-pyroglutamic acid; 5-NO₂-salicylaldehyde / propan-2-ol; H₂O / 48 h / 70 °C

4.1: 99 percent / Na₂CO₃ / dioxane; H₂O / 18 h / 20 °C

5.1: LiHMDS / tetrahydrofuran / 0 °C

5.2: tetrahydrofuran / 0 - 20 °C

6.1: 100 percent / HCl / ethyl acetate / 0 - 20 °C

7.1: 57 percent / NMM / dimethylformamide / 20 °C

With 4-methyl-morpholine; hydrogenchloride; N,N,N,N,-tetramethylethylenediamine; ammonia; iodine; sodium carbonate; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; ethanol; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; 3.2: racemate resolution;
DOI:10.1016/S0960-894X(02)00010-0

Reference yield:

: 3349-64-2,68253-36-1,100485-58-3
1-tetralone oxime

: 368426-47-5
[3-(2,3-dihydro-benzofuran-5-sulfonylamino)-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: PPA / 0.08 h / 115 °C

2.1: TMEDA; NaI / acetonitrile / -5 °C

3.1: 95 percent / I₂ / -5 - 20 °C

4.1: NH₃ / aq. ethanol / 0 - 20 °C

4.2: L-pyroglutamic acid; 5-NO₂-salicylaldehyde / propan-2-ol; H₂O / 48 h / 70 °C

5.1: 99 percent / Na₂CO₃ / dioxane; H₂O / 18 h / 20 °C

6.1: LiHMDS / tetrahydrofuran / 0 °C

6.2: tetrahydrofuran / 0 - 20 °C

7.1: 100 percent / HCl / ethyl acetate / 0 - 20 °C

8.1: 57 percent / NMM / dimethylformamide / 20 °C

With 4-methyl-morpholine; hydrogenchloride; N,N,N,N,-tetramethylethylenediamine; ammonia; iodine; sodium carbonate; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; ethanol; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; 4.2: racemate resolution;
DOI:10.1016/S0960-894X(02)00010-0