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Ethanolamine → 7-beta-D-galactopyranosyloxycoumarin-4-acetic acid-(2-hydroxyethyl)amide

HRID 610661
ノート
印刷プレビュー

反応式

HRID 610661 の反応式
C([O:4][C@@H:5]1[C@@H:10]([O:11]C(=O)C)[C@@H:9]([O:15]C(=O)C)[C@@H:8]([CH2:19][O:20]C(=O)C)[O:7][C@H:6]1[O:24][C:25]1[CH:34]=[C:33]2[C:28]([C:29]([CH2:36][C:37]([O-])=[O:38])=[CH:30][C:31](=[O:35])[O:32]2)=[CH:27][CH:26]=1)(=O)C.[CH2:40]([CH2:42][NH2:43])[OH:41]>C(Cl)Cl.CO.CCOCC>[OH:41][CH2:40][CH2:42][NH:43][C:37](=[O:38])[CH2:36][C:29]1[C:28]2[C:33](=[CH:34][C:25]([O:24][C@@H:6]3[O:7][C@H:8]([CH2:19][OH:20])[C@H:9]([OH:15])[C@H:10]([OH:11])[C@H:5]3[OH:4])=[CH:26][CH:27]=2)[O:32][C:31](=[O:35])[CH:30]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 700EthanolamineHCID 867549227-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyloxy)coumarin-4-acetate2 回

生成物 1

HCID 99541407-beta-D-galactopyranosyloxycoumarin-4-acetic acid-(2-hydroxyethyl)amide収率 37.1%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 3283Diethyl Ether溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

43 g (0.076 moles) of 7-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)coumarin-4-acetate (i.e. compound 1 prepared as described in Scheme 1) was dissolved in 430 ml of methylene chloride in a 1 liter RB flask. 43 ml (0.712 moles) of ethanolamine was dissolved in 43 ml of methanol and added to the above solution. The solution was stirred at room temperature for 60 hrs and the resulting solid residue was filtered and washed with 50 ml of methylene chloride. The solid was suspended in 250 ml of methanol and stored in the freezer for 12 hrs. The solid was filtered again and suspended in 700 ml of methanol and refluxed for 30 min. The cloudy suspension was cooled to room temperature, then further cooled in an ice bath and filtered. The wet solid thus obtained was suspended in 200 ml of ether and stirred for 30 min., then filtered and vacuum dried at room temperature to give 12 g of an off-white solid. The yield was 37%. The structure was confirmed by 1H NMR and MS (as in Example 1).

後処理

  1. additionadded to the above solution
  2. filtrationthe resulting solid residue was filtered
  3. washwashed with 50 ml of methylene chloride
  4. waitstored in the freezer for 12 hrs
  5. filtrationThe solid was filtered again
  6. temperaturerefluxed for 30 min
  7. temperatureThe cloudy suspension was cooled to room temperature
  8. temperaturefurther cooled in an ice bath
  9. filtrationfiltered
  10. customThe wet solid thus obtained
  11. stirringstirred for 30 min.
  12. filtrationfiltered
  13. customvacuum dried at room temperature

出典と根拠

ORDレコード
ord-81773609d59c4a23bdcf5304d2876e25
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05998593

反応ノート

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