Hydrochloric Acid → N-(heptan-4-yl)-2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)acetamide

HRID 2410616

反応式

HRID 2410616 の反応式
C1(N=C=NC2CCCCC2)CCCCC1.[OH:16][C:17]1[CH:27]=[CH:26][C:20]([CH:21]([OH:25])[C:22]([OH:24])=O)=[CH:19][C:18]=1[O:28][CH3:29].ON1C(=O)CCC1=O.[CH3:38][CH2:39][CH2:40][CH:41]([NH2:45])[CH2:42][CH2:43][CH3:44].C(=O)(O)[O-].[Na+].Cl>O1CCOCC1.O>[CH3:38][CH2:39][CH2:40][CH:41]([NH:45][C:22](=[O:24])[CH:21]([OH:25])[C:20]1[CH:26]=[CH:27][C:17]([OH:16])=[C:18]([O:28][CH3:29])[CH:19]=1)[CH2:42][CH2:43][CH3:44]

参加物

9

実験手順

A solution of dicyclohexyl carbodiimide (DCC) (5.5 g, 26.7 mmol) in 1,4-dioxane (50 ml) was added to a stirred solution of 4-hydroxy-3-methoxymandelic acid (5 g, 25.3 mmol) and N-hydroxysuccinimide (3 g, 26.1 mmol) in 1,4-dioxane (100 ml) at room temperature. The resulting white suspension was stirred at room temperature for 16 hours. Then the reaction mixture was filtered. The filtrate was poured into a stirred solution of 4-heptylamine in water (20 ml) and sodium bicarbonate (2.5 g, 20 mmol) was added. The resulting solution was heated to 50° C. and stirred at this temperature for 1.5 hour. The cooled solution was acidified to pH<2 using aq. HCl 5% solution and extracted three times with ethyl acetate (100 ml). The combined organic layers were washed with brine, dried with sodium sulfate, filtered and the filtrate concentrated by evaporation under reduced pressure. The residue was purified by crystallization from ethyl acetate/heptane to yield the title product (5.5 g, 73.6%) as white crystals.

後処理

  1. filtrationThen the reaction mixture was filtered
  2. additionwas added
  3. temperatureThe resulting solution was heated to 50° C.
  4. stirringstirred at this temperature for 1.5 hour
  5. extractionextracted three times with ethyl acetate (100 ml)
  6. washThe combined organic layers were washed with brine
  7. dry with materialdried with sodium sulfate
  8. filtrationfiltered
  9. concentrationthe filtrate concentrated by evaporation under reduced pressure
  10. customThe residue was purified by crystallization from ethyl acetate/heptane

出典と根拠

ORDレコード
ord-23bcf3ef293b4ed48b494c2058a26181
出典データセット
uspto-grants-2014_08
特許番号
US08816102B2

関連ノート

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