Dimethylamine, hydrochloride → HCID 22724191, compound

HRID 2086845Notes

Reaction equation

HRID 2086845 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

  1. washwashed with water
  2. customAfter removal of the solvents, crude residue
  3. 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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