Dimethylamine, hydrochloride → HCID 22724191, compound
Reaction equation
C1(=O)N([O:6][C:7]([CH2:9][CH2:10][C:11]2[C:16](=[O:17])[N:15]([C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([NH:24][C:25]([NH:27][C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=4[O:34][CH3:35])=[O:26])[CH:19]=3)[C:14]3[N:36]=[CH:37][CH:38]=[CH:39][C:13]=3[N:12]=2)=O)C(=O)CC1.Cl.[CH3:43][NH:44][CH3:45]>O1CCOCC1.O.C(N(CC)CC)C.C(OCC)(=O)C>[CH3:43][N:44]([CH3:45])[C:7]([CH2:9][CH2:10][C:11]1[C:16](=[O:17])[N:15]([C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([NH:24][C:25]([NH:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[O:34][CH3:35])=[O:26])[CH:19]=2)[C:14]2[N:36]=[CH:37][CH:38]=[CH:39][C:13]=2[N:12]=1)=[O:6]Participants
7
Procedure
To a solution of 2-[2-succinimidooxycarbonylethyl]-4-[3-[3-(2-methoxyphenyl)ureido]phenyl]-3-oxo-3,4-dihydropyrido[2,3-b]pyrazine (0.28 g) in dioxane was added a solution of dimethylamine hydrochloride (81 mg) in water and triethylamine (101 mg). The mixture was stirred for 18 hours, diluted with ethyl acetate, washed with water. After removal of the solvents, crude residue was crystallized from ethanol to give 2-[2-(N,N-dimethylcarbamoyl)ethyl]-3-oxo-4-[3-[3-(2-methoxyphenyl)-ureido]phenyl]-3,4-dihydropyrido[2,3-b]pyrazine.
Workup
- washwashed with water
- customAfter removal of the solvents, crude residue
- customwas crystallized from ethanol
Sources & evidence
- ORD record
- ord-ca50bd7bddb34251a934b9fa38ef56f4
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727245B2
Reaction notes
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