Sodium Hydroxide → HCID 67388966, compound
Reaction equation
C([O:3][C:4]([C:6]1[C:7]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([CH:20]([OH:22])[CH3:21])[CH:15]=2)=[N:8][C:9](Cl)=[N:10][CH:11]=1)=[O:5])C.Cl.[Cl:24][C:25]1[CH:26]=[C:27]([CH2:33][CH2:34][NH2:35])[CH:28]=[C:29]([Cl:32])[C:30]=1[OH:31].C(N(C(C)C)CC)(C)C.[OH-].[Na+]>CN1C(=O)CCC1.CO.C1COCC1>[Cl:24][C:25]1[CH:26]=[C:27]([CH2:33][CH2:34][NH:35][C:9]2[N:8]=[C:7]([NH:13][C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([CH:20]([OH:22])[CH3:21])[CH:15]=3)[C:6]([C:4]([OH:3])=[O:5])=[CH:11][N:10]=2)[CH:28]=[C:29]([Cl:32])[C:30]=1[OH:31]Participants
7
Procedure
2-Chloro-4-{[3-(1-hydroxyethyl)phenyl]amino}pyrimidine-5-carboxylic acid ethyl ester synthesized in accordance with the method described in WO 99/31073 and 2-(3,5-dichloro-4-hydroxyphenyl)ethylamine hydrochloride were allowed to undergo the reaction at 80 to 90° C. in NMP in the presence of diisopropylethylamine, and the resulting compound was allowed to react with 1 M sodium hydroxide aqueous solution under heating in a mixed methanol-THF solution to obtain 2-{[2-(3,5-dichloro-4-hydroxyphenyl)ethyl]amino}-4-{[3-(1-hydroxyethyl)phenyl]amino}pyrimidine-5-carboxylic acid. F: 463
Sources & evidence
- ORD record
- ord-85a5cab409e44f998978664a4bbf24d8
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449456B2
Reaction notes
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