2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

Base Information

Chemical Name:2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide
CAS No.:177559-76-1
Molecular Formula:C₂₆H₂₂N₂O₃
Molecular Weight:410.472
Hs Code.:

Synonyms:2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

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Technology Process of 2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

There total 8 articles about 2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide 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: 13.0%

: 177559-76-1
2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

Guidance literature:

Reference yield: 12.6%

: 177559-72-7
2-(2-Cyclopropyl-7-methoxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

: 177559-76-1
2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

Guidance literature:: With boron tribromide; In dichloromethane;
DOI:10.1021/jm960395q

Reference yield:

: 24103-75-1
4-methoxy-2-methylpyridine

: 177559-76-1
2-(2-Cyclopropyl-7-hydroxy-3-(o-phenylbenzyl)indolizin-1-yl)glyoxylamide

Guidance literature:: Multi-step reaction with 6 steps

1: 2.) 1,8-diazabicyclo<5.4.0>undec-7-ene / 1.) EtOAc, heating, 2.) benzene, reflux

2: benzene / 4 h / Heating

3: 44.3 percent / BH₃, t-BuNH₂, AlCl₃ / CH₂Cl₂ / 5 h

4: tetrahydrofuran / 1 h / 0 °C

5: aq. NH₄OH / tetrahydrofuran / 1 h / Ambient temperature

6: 12.6 percent / BBr₃ / CH₂Cl₂

With ammonium hydroxide; aluminium trichloride; borane; boron tribromide; 1,8-diazabicyclo[5.4.0]undec-7-ene; tert-butylamine; In tetrahydrofuran; dichloromethane; benzene;
DOI:10.1021/jm960395q