Sodium Hydroxide → N-(2-hydroxy-4-methoxybenzoyl)cysteamine

HRID 465917

반응식

HRID 465917 반응식
C(OC([O:6][C:7]1[CH:18]=[C:17]([O:19][CH3:20])[CH:16]=[CH:15][C:8]=1[C:9]([NH:11][CH2:12][CH2:13][SH:14])=[O:10])=O)C.[OH-].[Na+]>CO>[OH:6][C:7]1[CH:18]=[C:17]([O:19][CH3:20])[CH:16]=[CH:15][C:8]=1[C:9]([NH:11][CH2:12][CH2:13][SH:14])=[O:10]

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 14719509N-(2-ethoxycarbonyloxy-4-methoxybenzoyl)cysteamine

생성물 1

HCID 14719510N-(2-hydroxy-4-methoxybenzoyl)cysteamine수율 77%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4.50 g of the N-(2-ethoxycarbonyloxy-4-methoxybenzoyl)cysteamine was dissolved in 70 ml of methanol, and 17 ml of 2N aqueous solution of sodium hydroxide was added to the solution. The mixture was agitated for 45 minutes. The solvent was distilled off in evacuated atomosphere, and 2N aqueous solution of sodium hydroxide and methylene chloride were added to the mixture for separation. The aqueous phase was further washed with methylene chloride, acidified by adding 6N aqueous hydrochloric acid, and extracted with methylene chloride. The mixture was dried over anhydrous sodium sulfate, and the solvent was distilled off in evacuated atomosphere. The residue was subjected to column chromatography using silica gel, and there was obtained 2.63 g of N-(2-hydroxy-4-methoxybenzoyl)cysteamine (I).

후처리

  1. distillationThe solvent was distilled off in evacuated atomosphere, and 2N aqueous solution of sodium hydroxide and methylene chloride
  2. additionwere added to the mixture for separation
  3. washThe aqueous phase was further washed with methylene chloride
  4. additionby adding 6N aqueous hydrochloric acid
  5. extractionextracted with methylene chloride
  6. dry with materialThe mixture was dried over anhydrous sodium sulfate
  7. distillationthe solvent was distilled off in evacuated atomosphere

출처 및 근거

ORD 기록
ord-5a046f7703cc45c78a8c2b05cba0d8dc
출처 데이터셋
uspto-grants-1992_10
특허 번호
US05155106

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