9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime

Base Information

• Chemical Name: 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime
• CAS No.: 126149-67-5
• Molecular Formula: C₁₇H₁₁ClFN₃O₂
• Molecular Weight: 343.745

Synonyms:9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime

Chemical Property of 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime

Chemical Property:

Purity/Quality:

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Technology Process of 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime

There total 4 articles about 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime 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:

9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one (126149-66-4) → 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime (126149-67-5)

Guidance literature:

With potassium tert-butylate; isopentyl nitrite; In tetrahydrofuran;

DOI:10.1016/S0960-894X(99)00573-9

Reference yield:

5-chloro-2,3-dihydroindole (25658-80-4) → 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime (126149-67-5)

Guidance literature:

Multi-step reaction with 3 steps

1: BCl₃; AlCl₃ / 1,2-dichloro-ethane

2: pyridine

3: t-BuOK; iAmONO / tetrahydrofuran

With pyridine; aluminium trichloride; potassium tert-butylate; boron trichloride; isopentyl nitrite; In tetrahydrofuran; 1,2-dichloro-ethane; 1: Acylation / 2: Cyclocondensation / 3: Nitrosation;

DOI:10.1016/S0960-894X(99)00573-9

Reference yield:

2-fluorobenzonitrile (394-47-8) → 9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime (126149-67-5)

Guidance literature:

Multi-step reaction with 3 steps

1: BCl₃; AlCl₃ / 1,2-dichloro-ethane

2: pyridine

3: t-BuOK; iAmONO / tetrahydrofuran

With pyridine; aluminium trichloride; potassium tert-butylate; boron trichloride; isopentyl nitrite; In tetrahydrofuran; 1,2-dichloro-ethane; 1: Acylation / 2: Cyclocondensation / 3: Nitrosation;

DOI:10.1016/S0960-894X(99)00573-9

upstream raw materials:

9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one

5-chloro-2,3-dihydroindole

2-fluorobenzonitrile

5-chloro-7-(2-fluorobenzoyl)indoline

Downstream raw materials:

3-amino-9-chloro-1-(2-fluoro-phenyl)-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one

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