4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide

Base Information

Chemical Name:4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide
CAS No.:1332388-86-9
Molecular Formula:C₂₂H₂₀FN₅O₂S
Molecular Weight:437.498
Hs Code.:

Synonyms:4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide

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Chemical Property of 4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide

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Technology Process of 4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide

There total 2 articles about 4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide 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:

: 915087-34-2
N-methyl-4-(1-cyanocyclopentylamino)-2-fluorobenzamide

: 463-71-8
thiophosgene

: 252056-70-5
5-amino-3-methylpyridine-2-carbonitrile

: 1332388-86-9
4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide

Guidance literature:: N-methyl-4-(1-cyanocyclopentylamino)-2-fluorobenzamide; thiophosgene; 5-amino-3-methylpyridine-2-carbonitrile; In N,N-dimethyl acetamide; at 60 ℃; Inert atmosphere;

With hydrogenchloride; water; In methanol; N,N-dimethyl acetamide; for 2h; Reflux;

Reference yield:

: 20970-75-6
2-cyano-3-methylpyridine

: 1332388-86-9
4-[7-(6-cyano-5-methyl-3-pyridyl)-6-oxo-8-thioxo-7,9-diazaspiro[4.4]nonan-9-yl]-2-fluoro-N-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrabutylammonium nitrate; trifluoroacetic anhydride / dichloromethane / 72 h / 0 - 20 °C

2.1: hydrogen / palladium on activated charcoal / methanol

3.1: N,N-dimethyl acetamide / 60 °C / Inert atmosphere

3.2: 2 h / Reflux

With hydrogen; tetrabutylammonium nitrate; trifluoroacetic anhydride; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl acetamide;