5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

Base Information

Chemical Name:5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester
CAS No.:690657-26-2
Molecular Formula:C₃₉H₄₃N₃O₆
Molecular Weight:649.787
Hs Code.:

5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5<i>H</i>-[1]pyrindine-6-carboxylic acid <i>tert</i>-butyl ester

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Chemical Property of 5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

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Technology Process of 5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

There total 10 articles about 5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl 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:

: 6620-80-0
N-isopropylbenzimidoyl chloride

: 690657-26-2
5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / CHCl₃ / Heating

2: 88 percent / aq. NaOH / methanol / 20 °C

3: NaI / acetonitrile

4: acetonitrile; methanol / 20 °C

With sodium hydroxide; triethylamine; sodium iodide; In methanol; chloroform; acetonitrile;
DOI:10.1016/j.bmcl.2004.01.008

Reference yield:

: 5-benzo[1,3]dioxol-5-yl-7-(2-formyl-4-methoxy-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

: 690657-26-2
5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: NaBH₄ / methanol / 0 °C

2: 65 percent / Et₃N; 4-dimethylaminopyridine / CHCl₃ / 20 °C

3: m-chloroperbenzoic acid / CHCl₃ / 0 °C

4: Et₃N / CHCl₃ / Heating

5: 88 percent / aq. NaOH / methanol / 20 °C

6: NaI / acetonitrile

7: acetonitrile; methanol / 20 °C

With dmap; sodium hydroxide; sodium tetrahydroborate; triethylamine; 3-chloro-benzenecarboperoxoic acid; sodium iodide; In methanol; chloroform; acetonitrile;
DOI:10.1016/j.bmcl.2004.01.008

Reference yield:

: 5-benzo[1,3]dioxol-5-yl-7-(2-hydroxymethyl-4-methoxy-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

: 690657-26-2
5-benzo[1,3]dioxol-5-yl-2-(benzoyl-isopropyl-amino)-7-(4-methoxy-2-methylaminomethyl-phenyl)-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 65 percent / Et₃N; 4-dimethylaminopyridine / CHCl₃ / 20 °C

2: m-chloroperbenzoic acid / CHCl₃ / 0 °C

3: Et₃N / CHCl₃ / Heating

4: 88 percent / aq. NaOH / methanol / 20 °C

5: NaI / acetonitrile

6: acetonitrile; methanol / 20 °C

With dmap; sodium hydroxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; sodium iodide; In methanol; chloroform; acetonitrile;
DOI:10.1016/j.bmcl.2004.01.008