Propyl mercaptan → HCID 86658684、化合物

HRID 42695

反応式

HRID 42695 の反応式
[CH2:1]([SH:4])[CH2:2][CH3:3].[H-].[Na+].Cl[C:8]1[N:13]([CH3:14])[C:12](=[O:15])[N:11]([CH3:16])[C:10](=[O:17])[C:9]=1[CH:18]=[O:19]>O1CCOCC1>[CH3:14][N:13]1[C:8]([S:4][CH2:1][CH2:2][CH3:3])=[C:9]([CH:18]=[O:19])[C:10](=[O:17])[N:11]([CH3:16])[C:12]1=[O:15]

参加物

5

実験手順

To a stirred solution of propane-1-thiol (2.30 mmol) in dry 1,4-dioxane (4 ml), NaH (2.30 mmol) was added under argon. To the mixture, a solution of 6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (2 mmol) in dry 1,4-dioxane (8 ml) was added at 5-8° C. in one portion. The mixture was stirred at room temperature until the starting material was consumed (monitored by TLC). Then the mixture was poured onto ice water (50 ml) and the aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phases were washed with water and dried over anhydrous MgSO4. The solvent was evaporated in vacuo and the crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent.

後処理

  1. customwas consumed (monitored by TLC)
  2. additionThen the mixture was poured onto ice water (50 ml)
  3. extractionthe aqueous phase was extracted with ethyl acetate (3×30 ml)
  4. washThe combined organic phases were washed with water
  5. dry with materialdried over anhydrous MgSO4
  6. customThe solvent was evaporated in vacuo
  7. customthe crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent

出典と根拠

ORDレコード
ord-36c7cc926e514e7ea932e77118df6091
出典データセット
uspto-grants-2013_09
特許番号
US08536210B2

関連ノート

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