Sodium Hydroxide → HCID 71555923, compound
Reaction equation
C([O:3][C:4]([C:6]1[C:7]([N:25]([CH2:28][CH3:29])[CH2:26][CH3:27])=[N:8][C:9]2[C:14]([C:15]=1[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[Cl:23])=[CH:13][C:12]([Cl:24])=[CH:11][CH:10]=2)=[O:5])C.[OH-].[Na+]>>[Cl:24][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([N:25]([CH2:28][CH3:29])[CH2:26][CH3:27])[C:6]([C:4]([OH:5])=[O:3])=[C:15]2[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[Cl:23]Participants
3
Procedure
The title compound was prepared in analogy to example 12 step B from a mixture of 6-chloro-4-(2-chloro-benzyl)-2-diethylamino-quinoline-3-carboxylic acid ethyl ester (50 mg, 0.116 mmol) and 1N NaOH. Pale yellow solid (32 mg, 68%). LC-MS (ESI): 403 (M+H)+.
Sources & evidence
- ORD record
- ord-601d605036c247428e783aaf46fd9ba1
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09199938B2
Reaction notes
Loading…