6-(cyclopropylmethyl)-5-methyl-4,5,6,7-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one

Base Information

Chemical Name:6-(cyclopropylmethyl)-5-methyl-4,5,6,7-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one
CAS No.:126234-01-3
Molecular Formula:C15H19N3O
Molecular Weight:257.3309
Hs Code.:
Mol file:126234-01-3.mol

Synonyms:Imidazo(4,5,1-jk)(1,4)benzodiazepin-2(1H)-one, 6-(cyclopropylmethyl)-4,5,6,7-tetrahydro-5-methyl-;6-(Cyclopropylmethyl)-4,5,6,7-tetrahydro-5-methylimidazo(4,5,1-jk)(1,4)benzodiazepin-2(1H)-one;

Suppliers and Price of 6-(cyclopropylmethyl)-5-methyl-4,5,6,7-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of 6-(cyclopropylmethyl)-5-methyl-4,5,6,7-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one

Chemical Property:

Refractive Index:1.661
Density:1.29g/cm³

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 6-(cyclopropylmethyl)-5-methyl-4,5,6,7-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one

There total 8 articles about 6-(cyclopropylmethyl)-5-methyl-4,5,6,7-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-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: 78.0%

: 126233-79-2
4,5,6,7-tetrahydro-5-methylimidazo<4,5,1-jk><1,4>benzodiazepin-2(1H)-one

: 7051-34-5
cyclopropylcarbinyl bromide

: 126234-01-3
7-Cyclopropylmethyl-8-methyl-6,7,8,9-tetrahydro-2H-2,7,9a-triaza-benzo[cd]azulen-1-one

Guidance literature:: With sodium carbonate; potassium iodide; In N,N-dimethyl-formamide; for 22.5h; Ambient temperature;
DOI:10.1021/jm00106a040

Reference yield:

: 6286-36-8
2-bromo-3-nitrobenzoic acid chloride

: 126234-01-3
7-Cyclopropylmethyl-8-methyl-6,7,8,9-tetrahydro-2H-2,7,9a-triaza-benzo[cd]azulen-1-one

Guidance literature:: Multi-step reaction with 7 steps

1: 1 h / Heating

2: Na₂CO₃ / butan-1-ol / 1.5 h / Heating

3: 93 percent / 2-hydroxypyridine / xylene / 19 h / Heating

4: lithium aluminum hydride, conc. H₂SO₄ / tetrahydrofuran / 24 h

5: 71 percent / tetrahydrofuran / 1.) 0 deg C, 10 min, 2.) RT, 1 h

6: 87 percent / H₂ / 10percent Pd/C / acetic acid / 6 h / 42 °C / 3102.9 Torr

7: 78 percent / potassium iodide, sodium carbonate / dimethylformamide / 22.5 h / Ambient temperature

With 2-hydroxypyridin; lithium aluminium tetrahydride; sulfuric acid; hydrogen; sodium carbonate; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; acetic acid; N,N-dimethyl-formamide; xylene; butan-1-ol;
DOI:10.1021/jm00106a040

Reference yield:

: 573-54-6
2-bromo-3-nitro-benzoic acid

: 126234-01-3
7-Cyclopropylmethyl-8-methyl-6,7,8,9-tetrahydro-2H-2,7,9a-triaza-benzo[cd]azulen-1-one

Guidance literature:: Multi-step reaction with 8 steps

1: thionyl chloride / toluene / 2 h / Heating

2: 1 h / Heating

3: Na₂CO₃ / butan-1-ol / 1.5 h / Heating

4: 93 percent / 2-hydroxypyridine / xylene / 19 h / Heating

5: lithium aluminum hydride, conc. H₂SO₄ / tetrahydrofuran / 24 h

6: 71 percent / tetrahydrofuran / 1.) 0 deg C, 10 min, 2.) RT, 1 h

7: 87 percent / H₂ / 10percent Pd/C / acetic acid / 6 h / 42 °C / 3102.9 Torr

8: 78 percent / potassium iodide, sodium carbonate / dimethylformamide / 22.5 h / Ambient temperature

With 2-hydroxypyridin; lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; hydrogen; sodium carbonate; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; acetic acid; N,N-dimethyl-formamide; toluene; xylene; butan-1-ol;
DOI:10.1021/jm00106a040