1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Base Information

Chemical Name:1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one
CAS No.:197368-83-5
Molecular Formula:C₁₇H₁₅N₃O₃
Molecular Weight:309.324
Hs Code.:

Synonyms:1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

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Chemical Property of 1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

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Technology Process of 1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

There total 4 articles about 1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-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:

Reference yield: 25.0%

: 877171-08-9
3,5-dihydro-5-methyl-7,8-methylenedioxy-1-(4-nitrophenyl)-4H-2,3-benzodiazepin-4-one

: 197368-83-5
1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Guidance literature:: With ammonium formate; nickel; In ethanol; for 2h; Heating;
DOI:10.1021/jm050552y

Reference yield:

: 126934-94-9,24314-70-3
methyl 2-(3,4-methylenedioxyphenyl)propionate

: 197368-83-5
1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 33 percent / phosphorus pentoxide / 1,2-dichloro-ethane / 20 °C

2: 20 percent / hydrazine hydrate / butan-1-ol / 20 h / Heating

3: 25 percent / ammonium formate; Raney Ni / ethanol / 2 h / Heating

With phosphorus pentaoxide; ammonium formate; nickel; hydrazine hydrate; In ethanol; 1,2-dichloro-ethane; butan-1-ol; 1: Friedel-Crafts acylation;
DOI:10.1021/jm050552y

Reference yield:

: 326-59-0
benzo[1,3]dioxol-5-yl-acetic acid methyl ester

: 197368-83-5
1-(4-aminophenyl)-5-methyl-7,8-methylenedioxy-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium hydride / tetrahydrofuran / 0.5 h / -70 °C

1.2: 86.8 percent / tetrahydrofuran / 16 h / -70 - 20 °C

2.1: 33 percent / phosphorus pentoxide / 1,2-dichloro-ethane / 20 °C

3.1: 20 percent / hydrazine hydrate / butan-1-ol / 20 h / Heating

4.1: 25 percent / ammonium formate; Raney Ni / ethanol / 2 h / Heating

With phosphorus pentaoxide; ammonium formate; potassium hydride; nickel; hydrazine hydrate; In tetrahydrofuran; ethanol; 1,2-dichloro-ethane; butan-1-ol; 2.1: Friedel-Crafts acylation;
DOI:10.1021/jm050552y