4-Chlorobenzylamine → HCID 178522877, compound
Reaction equation
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:16]([F:19])([F:18])[F:17])=[CH:9][C:10]=2[C:12]([F:15])([F:14])[F:13])[N:5]=[CH:4][C:3]=1[C:20](OCC)=[O:21].[Cl:25][C:26]1[CH:33]=[CH:32][C:29]([CH2:30][NH2:31])=[CH:28][CH:27]=1>>[Cl:25][C:26]1[CH:33]=[CH:32][C:29]([CH2:30][NH:31][C:20]([C:3]2[CH:4]=[N:5][C:6]3[C:7]([C:2]=2[OH:1])=[C:8]([C:16]([F:18])([F:19])[F:17])[CH:9]=[C:10]([C:12]([F:13])([F:15])[F:14])[CH:11]=3)=[O:21])=[CH:28][CH:27]=1Participants
Conditions
- Temperature
- 200 °C
Procedure
A mixture of 0.35 g of ethyl 4-hydroxy-5,7-bis(trifluoromethyl)-3-quinolinecarboxylate (FR 2537140) and 3.0 mL of 4-chlorobenzylamine is stirred 1 h at 200° C. The mixture is cooled to 25° C. and it is diluted with 25 mL of hexanes. After stirring for an additional 1 h the solid precipitate is collected by filtration and washed with 10 mL of hexanes. It is dried in a stream of air and then it is suspended in 20 mL of glacial acetic acid. The mixture is heated until the solid is completely dissolved and the resulting solution is diluted with 200 mL of distilled water. The mixture is allowed to cool to 25° C. and the solid is collected by filtration. It is washed with a small volume of 10% aqueous acetic acid and then it is dried at torr and 45° C. for 18 h. The yield is 0.23 g.
Workup
- temperatureThe mixture is cooled to 25° C.
- stirringAfter stirring for an additional 1 h the solid precipitate
- filtrationis collected by filtration
- washwashed with 10 mL of hexanes
- customIt is dried in a stream of air
- temperatureThe mixture is heated until the solid
- dissolutionis completely dissolved
- additionthe resulting solution is diluted with 200 mL of distilled water
- temperatureto cool to 25° C.
- filtrationthe solid is collected by filtration
- washIt is washed with a small volume of 10% aqueous acetic acid
- customit is dried at torr and 45° C. for 18 h
Sources & evidence
- ORD record
- ord-fd807776a10b44d79ffbf518d8d599bb
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06093732
Reaction notes
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