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Bromoacetic Acid → 10-[2-[[2-(2-Hydroxyethoxy)ethyl]amino]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-1,4,7,10-tetraazacyclododecan-1,4,7-triacetic acid

HRID 54160
ノート
印刷プレビュー

反応式

HRID 54160 の反応式
Br[CH2:2][C:3]([OH:5])=[O:4].[OH-:6].[Na+].Cl.Cl.Cl.[C:11]1([CH2:17][O:18][CH2:19][CH:20]([N:24]2[CH2:35][CH2:34][NH:33][CH2:32][CH2:31][NH:30][CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)[C:21]([NH2:23])=[O:22])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>O>[OH:6][CH2:11][CH2:17][O:18][CH2:19][CH2:20][NH:23][C:21](=[O:22])[CH:20]([N:24]1[CH2:35][CH2:34][N:33]([CH2:2][C:3]([OH:5])=[O:4])[CH2:32][CH2:31][N:30]([CH2:2][C:3]([OH:5])=[O:4])[CH2:29][CH2:28][N:27]([CH2:2][C:3]([OH:5])=[O:4])[CH2:26][CH2:25]1)[CH2:19][O:18][CH2:17][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6227Bromoacetic AcidHCID 14798Sodium Hydroxide3 回HCID 86750719alpha-[(Phenylmethoxy)methyl]-1,4,7,10-tetraazacyclododecan-1-acetamide trihydrochloride

生成物 1

HCID 1971050910-[2-[[2-(2-Hydroxyethoxy)ethyl]amino]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-1,4,7,10-tetraazacyclododecan-1,4,7-triacetic acid収率 150%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
2 回

反応条件

温度
0 °C

実験手順

To a solution of 45.5 g of bromoacetic acid (0.327 mol) in 140 mL of H2O, kept under stirring at 0° C., 31.5 mL of 10N NaOH (0.315 mol) are added in 1 h to pH 6. The resulting solution is added drop by drop to a solution of 46 g of N-[2-(2-hydroxyethoxy)ethyl)]-α-[(phenylmethoxy)methyl]-1,4,7,10-tetraazacyclododecan-1-acetamide trihydrochloride (0.084 mol) in H2O (100 mL) and, at a constant reaction temperature of 0° C., 10N NaOH is slowly added to pH 10. The reaction mixture is heated to 50° C. for 48 h and 50 mL of 10N NaOH (0.5 mol) are added to keep a constant pH of 10. After cooling at room temperature, the mixture is filtered on a MilliporeR filter, neutralized with 37%HCl (w/w), diluted to 1.5 L with H2O and electrodialyzed. When the electrodialysis is over, the solution is concentrated under vacuum to give an oily residue which is placed into a drier to give a glassy solid. The solid is triturated and dissolved with AcOEt (200 mL), filtered and dried again. The crude product is dissolved in H2O (150 mL) and percolated on Amberlite® XAD 16 resin (1000 mL) performing a gradient elution with H2O-MeOH. The fractions containing the pure product are collected and concentrated under vacuum to give 38.83 g of the desired product (0.063 mol).

後処理

  1. temperatureThe reaction mixture is heated to 50° C. for 48 h
  2. temperatureAfter cooling at room temperature
  3. filtrationthe mixture is filtered on a MilliporeR
  4. filtrationfilter
  5. additiondiluted to 1.5 L with H2O
  6. concentrationis concentrated under vacuum
  7. customto give an oily residue which
  8. customto give a glassy solid
  9. customThe solid is triturated
  10. dissolutiondissolved with AcOEt (200 mL)
  11. filtrationfiltered
  12. customdried again
  13. dissolutionThe crude product is dissolved in H2O (150 mL)
  14. washa gradient elution with H2O-MeOH
  15. additionThe fractions containing the pure product
  16. customare collected
  17. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-9a7c0abf2055454299b30f5fa8233fa9
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05622688

反応ノート

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