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

Base Information

Chemical Name:7,8-methylenedioxy-1-(4-nitrophenyl)-3,5-dihydro-2,3-benzodiazepin-4(4H)-one
CAS No.:194729-10-7
Molecular Formula:C₁₆H₁₁N₃O₅
Molecular Weight:325.28
Hs Code.:

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

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

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

There total 7 articles about 7,8-methylenedioxy-1-(4-nitrophenyl)-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: 75.0%

: 194729-09-4
2-(4-nitro-benzoyl)-4,5-(methylenedioxy)-phenyl acetic acid

: 194729-10-7
7,8-methylenedioxy-1-(4-nitrophenyl)-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Guidance literature:: 2-(4-nitro-benzoyl)-4,5-(methylenedioxy)-phenyl acetic acid; With triethylamine; isobutyl chloroformate; In tetrahydrofuran; at -20 ℃;

With hydrazine hydrate; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jm0580003

Reference yield: 55.0%

: 197369-14-5
2-(4-nitrobenzoyl)-4,5-methylenedioxyphenylacetic acid methyl ester

: 194729-10-7
7,8-methylenedioxy-1-(4-nitrophenyl)-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Guidance literature:: With hydrazine hydrate; In ethanol; for 5h; Heating;
DOI:10.1021/jm980168j

Reference yield:

: 2861-28-1
1,3-benzodioxole-5-acetic acid

: 194729-10-7
7,8-methylenedioxy-1-(4-nitrophenyl)-3,5-dihydro-2,3-benzodiazepin-4(4H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 95 percent / LiAlH₄ / diethyl ether; tetrahydrofuran / 8 h / 20 °C

2.1: 83 percent / aq. HCl / toluene / 20 °C

3.1: 52 percent / aq. H₂SO₄; CrO₃ / acetone / 15 - 20 °C

4.1: Et₃N; isobutyl chloroformate / tetrahydrofuran / -20 °C

4.2: 75 percent / hydrazine hydrate / tetrahydrofuran / 20 °C

With chromium(VI) oxide; hydrogenchloride; lithium aluminium tetrahydride; sulfuric acid; triethylamine; isobutyl chloroformate; In tetrahydrofuran; diethyl ether; acetone; toluene; 3.1: Jones oxidation;
DOI:10.1021/jm0580003