Technology Process of 4-[2-(1-aminomethylcyclopropylmethoxy)-3,4-dimethoxyphenyl]indan-1-one
There total 11 articles about 4-[2-(1-aminomethylcyclopropylmethoxy)-3,4-dimethoxyphenyl]indan-1-one 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:
- Guidance literature:
-
4-(2-((1-(azidomethyl)cyclopropyl)methoxy)-3,4-dimethoxyphenyl)-2,3-dihydro-1H-inden-1-one;
With
triphenylphosphine;
In
tetrahydrofuran;
at 20 ℃;
for 2h;
With
water;
In
tetrahydrofuran;
at 80 ℃;
for 1h;
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: N-Bromosuccinimide / tetrahydrofuran / 1 h / 20 - 25 °C
2.1: triethylamine / dichloromethane / 1 h / 0 - 20 °C
3.1: n-butyllithium / tetrahydrofuran / 0.33 h / -78 °C
3.2: 0.5 h / -78 °C
4.1: caesium carbonate / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 4 h / 90 °C / Inert atmosphere
5.1: hydrogenchloride; water / methanol / 0.25 h / 50 °C
6.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 20 °C
7.1: tetrabutyl ammonium fluoride / trifluoroacetic acid-d1 / 16 h / 20 °C
8.1: triethylamine / dichloromethane / 1 h / 0 - 20 °C
9.1: sodium azide / N,N-dimethyl-formamide / 16 h / 20 °C
10.1: triphenylphosphine / tetrahydrofuran / 2 h / 20 °C
10.2: 1 h / 80 °C
With
hydrogenchloride; N-Bromosuccinimide; n-butyllithium; sodium azide; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; water; caesium carbonate; triethylamine; triphenylphosphine;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; methanol; dichloromethane; trifluoroacetic acid-d1; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: n-butyllithium / tetrahydrofuran / 0.33 h / -78 °C
1.2: 0.5 h / -78 °C
2.1: caesium carbonate / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 4 h / 90 °C / Inert atmosphere
3.1: hydrogenchloride; water / methanol / 0.25 h / 50 °C
4.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 20 °C
5.1: tetrabutyl ammonium fluoride / trifluoroacetic acid-d1 / 16 h / 20 °C
6.1: triethylamine / dichloromethane / 1 h / 0 - 20 °C
7.1: sodium azide / N,N-dimethyl-formamide / 16 h / 20 °C
8.1: triphenylphosphine / tetrahydrofuran / 2 h / 20 °C
8.2: 1 h / 80 °C
With
hydrogenchloride; n-butyllithium; sodium azide; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; water; caesium carbonate; triethylamine; triphenylphosphine;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; methanol; dichloromethane; trifluoroacetic acid-d1; N,N-dimethyl-formamide;