Hydrochloric Acid → HCID 444698、化合物

HRID 1584563ノート

反応式

HRID 1584563 の反応式
[OH-].[Na+].[CH2:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6][C@H:5]([C:13]([OH:15])=[O:14])[NH:4]1.[C:16]1([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1.Cl>O.O1CCCC1>[C:16]1([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:21]=[CH:20][C:19]([S:22]([N:4]2[C@@H:5]([C:13]([OH:15])=[O:14])[CH2:6][C:7]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH2:3]2)(=[O:24])=[O:23])=[CH:18][CH:17]=1

参加物

7

実験手順

Sodium hydroxide (13.6 g) is dissolved in water (300 ml), and therein is suspended (3R)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid (30.0 g) and thereto is added tetrahydrofuran (120 ml). To the resulting solution is added 4-biphenylylsulfonyl chloride (42.9 g), and the mixture is stirred at room temperature for one hour. The reaction mixture is acidified with 10% hydrochloric acid under ice cooling, and is diluted with water, and then extracted twice with ethyl acetate. The extract is washed with water and an aqueous saturated saline solution, dried over sodium sulfate and then treated with active carbon. Undissolved materials are filtered off from the extract, and the solvent is distilled off under reduced pressure. The residue is recrystallized from ethyl acetate-hexane to give (3R)-N-(4-biphenylylsulfonyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid (36.5 g) as colorless crystals.

後処理

  1. extractionextracted twice with ethyl acetate
  2. washThe extract is washed with water
  3. dry with materialan aqueous saturated saline solution, dried over sodium sulfate
  4. additiontreated with active carbon
  5. filtrationUndissolved materials are filtered off from the extract
  6. distillationthe solvent is distilled off under reduced pressure
  7. customThe residue is recrystallized from ethyl acetate-hexane

出典と根拠

ORDレコード
ord-f40be8abb5b246638e28630feabaf0ea
出典データセット
uspto-grants-1999_08
特許番号
US05932732

反応ノート

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