2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

Base Information

Chemical Name:2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid
CAS No.:1262007-55-5
Molecular Formula:C₂₄H₂₄N₂O₅
Molecular Weight:420.465
Hs Code.:

Synonyms:2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

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Chemical Property of 2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

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Technology Process of 2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

There total 13 articles about 2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid 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:

: 1262008-29-6
ethyl 2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetate

: 1262007-55-5
2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

Guidance literature:: ethyl 2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetate; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃; for 2h;

With hydrogenchloride; In tetrahydrofuran; methanol; water;

Reference yield:

: ethyl 3-(5-(benzyloxy)-1-(2-(tert-butyldimethylsilyloxy)ethyl)-1H-indol-2-yl)acrylate

: 1262007-55-5
2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C

2: potassium tert-butylate / toluene; tetrahydrofuran / 1.5 h / 60 °C / microwave irradiation

3: hydrogen / 20 % Pd(OH)2/C / ethyl acetate / 2 h / 2068.65 Torr

4: caesium carbonate / ISOPROPYLAMIDE / 3 h / 60 °C / microwave irradiation

5: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 2 h / 20 °C

With lithium hydroxide monohydrate; potassium tert-butylate; tetrabutyl ammonium fluoride; water; hydrogen; caesium carbonate; 20 % Pd(OH)2/C; In tetrahydrofuran; methanol; ISOPROPYLAMIDE; ethyl acetate; toluene;

Reference yield:

: ethyl 3-(5-(benzyloxy)-1-(2-hydroxyethyl)-1H-indol-2-yl)acrylate

: 1262007-55-5
2-(8-(3-cyano-4-isopropoxybenzyloxy)-3,4-dihydro-1H-[1,4]oxazino[4,3-a]indol-1-yl)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: potassium tert-butylate / toluene; tetrahydrofuran / 1.5 h / 60 °C / microwave irradiation

2: hydrogen / 20 % Pd(OH)2/C / ethyl acetate / 2 h / 2068.65 Torr

3: caesium carbonate / ISOPROPYLAMIDE / 3 h / 60 °C / microwave irradiation

4: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 2 h / 20 °C

With lithium hydroxide monohydrate; potassium tert-butylate; water; hydrogen; caesium carbonate; 20 % Pd(OH)2/C; In tetrahydrofuran; methanol; ISOPROPYLAMIDE; ethyl acetate; toluene;