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Potassium Carbonate → N,N'-bis[2,3-bis(acetyloxy)propyl]-5-(3-bromo-2-oxo-1-piperidinyl]-2,4,6-triiodo-1,3-benzenedicarboxamide

HRID 977803
ノート
印刷プレビュー

反応式

HRID 977803 の反応式
[C:1]([O:4][CH:5]([CH2:42][O:43][C:44](=[O:46])[CH3:45])[CH2:6][NH:7][C:8]([C:10]1[C:15]([I:16])=[C:14]([NH:17][C:18](=[O:25])[CH:19]([Br:24])[CH2:20][CH2:21][CH2:22]Br)[C:13]([I:26])=[C:12]([C:27]([NH:29][CH2:30][CH:31]([O:37][C:38](=[O:40])[CH3:39])[CH2:32][O:33][C:34](=[O:36])[CH3:35])=[O:28])[C:11]=1[I:41])=[O:9])(=[O:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>CN(C)C(=O)C.C(OCC)(=O)C>[C:1]([O:4][CH:5]([CH2:42][O:43][C:44](=[O:46])[CH3:45])[CH2:6][NH:7][C:8]([C:10]1[C:15]([I:16])=[C:14]([N:17]2[CH2:22][CH2:21][CH2:20][CH:19]([Br:24])[C:18]2=[O:25])[C:13]([I:26])=[C:12]([C:27]([NH:29][CH2:30][CH:31]([O:37][C:38](=[O:40])[CH3:39])[CH2:32][O:33][C:34](=[O:36])[CH3:35])=[O:28])[C:11]=1[I:41])=[O:9])(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 11430Potassium CarbonateHCID 19048400N,N'-bis[2,3-bis(acetyloxy)propyl]-5-[(2,5-dibromo-1-oxopentyl)amino]-2,4,6-triiodo-1,3-benzenedicarboxamide

生成物 1

HCID 19048418N,N'-bis[2,3-bis(acetyloxy)propyl]-5-(3-bromo-2-oxo-1-piperidinyl]-2,4,6-triiodo-1,3-benzenedicarboxamide収率 80%

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒
HCID 31374
Dimethylacetamide
溶媒

実験手順

To a solution of N,N'-bis[2,3-bis(acetyloxy)propyl]-5-[(2,5-dibromo-1-oxopentyl)amino]-2,4,6-triiodo-1,3-benzenedicarboxamide of example 8a (20.7 g, 18.5 mmol) in N,N-dimethylacetamide (200 ml), was added powdered potassium carbonate (20 g, 92 mmol) and the mixture was stirred at room temperature for 5 hours. The resulting slurry was filtered and the filtrate freed of the solvent to obtain a light brown solid, which was redissolved in ethyl acetate (500 ml). The solution was washed with water (2×50 ml) and saturated aqueous sodium chloride (1×100 ml) and then dried over magnesium sulfate. The solvent was removed in vacuo and the crude product (18.1 g) purified by column chromatography over silica gel to obtain pure N,N'-bis[2,3-bis(acetyloxy)propyl]-5-(3-bromo-2-oxo-1-piperidinyl]-2,4,6-triiodo-1,3-benzenedicarboxamide as a white solid (14.04 g, 80% yield), m.p. 232°-35°.

後処理

  1. filtrationThe resulting slurry was filtered
  2. customto obtain a light brown solid, which
  3. washThe solution was washed with water (2×50 ml) and saturated aqueous sodium chloride (1×100 ml)
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was removed in vacuo
  6. customthe crude product (18.1 g) purified by column chromatography over silica gel

出典と根拠

ORDレコード
ord-d32dc2ab02d94d06941f7788f1fc54e7
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05614638

反応ノート

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