1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

Base Information

Chemical Name:1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone
CAS No.:405168-04-9
Molecular Formula:C₂₂H₂₂N₂O₄
Molecular Weight:378.428
Hs Code.:

Synonyms:1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

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Chemical Property of 1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

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Technology Process of 1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

There total 7 articles about 1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone 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: 97.0%

: 405168-03-8
1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-phthalimidoethanone

: 405168-04-9
1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

Guidance literature:: With potassium hydroxide; In propan-1-ol; water; for 32h;
DOI:10.1080/00304940109356622

Reference yield:

: 479-59-4
julolidine

: 405168-04-9
1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / POCl₃

2: 79 percent / NH₂OH*HCl; AcONa*3H₂O / ethanol; H₂O / 24 h / 70 °C

3: 58 percent / Ac₂O / 3 h / Heating

4: 32 percent / diethyl ether / 2 h / Heating

5: 4.4 g / 40 percent HBr; Br₂ / 20 °C

6: 1.02 g / dimethylformamide / 96 h / 60 °C

7: 97 percent / KOH / H₂O; propan-1-ol / 32 h

With potassium hydroxide; hydroxylamine hydrochloride; hydrogen bromide; bromine; sodium acetate; acetic anhydride; trichlorophosphate; In propan-1-ol; diethyl ether; ethanol; water; N,N-dimethyl-formamide; 1: Vilsmeier reaction;
DOI:10.1080/00304940109356622

Reference yield:

: 97315-60-1
9-cyano-2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine

: 405168-04-9
1-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)-2-(2-carboxybenzamido)ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: 32 percent / diethyl ether / 2 h / Heating

2: 4.4 g / 40 percent HBr; Br₂ / 20 °C

3: 1.02 g / dimethylformamide / 96 h / 60 °C

4: 97 percent / KOH / H₂O; propan-1-ol / 32 h

With potassium hydroxide; hydrogen bromide; bromine; In propan-1-ol; diethyl ether; water; N,N-dimethyl-formamide;
DOI:10.1080/00304940109356622