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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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1-(3-Acetylthiopropanoyl)-L-proline → 1-(3-Mercapto-1-oxopropyl)-L-proline

HRID 2071382
ノート
印刷プレビュー

反応式

HRID 2071382 の反応式
C([S:4][CH2:5][CH2:6][C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8])(=O)C>N>[SH:4][CH2:5][CH2:6][C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 132083011-(3-Acetylthiopropanoyl)-L-proline

生成物 1

HCID 999781-(3-Mercapto-1-oxopropyl)-L-proline

試薬・触媒・溶媒 1

HCID 222Ammonia溶媒

実験手順

1-(3-Acetylthiopropanoyl)-L-proline (0.8 g.) is dissolved in 5.5 N methanolic ammonia (5 ml.) and the solution kept under argon at room temperature. After 2 hours the solvent is removed in vacuo, the residue is dissolved in water and applied to an ion exchange column on the H+ cycle [Dowex 50 (Analytical grade)] and eluted with water. The fractions that give thiol positive reaction are pooled and concentrated to dryness, yield 0.6 g. This product is crystallized from ethyl acetate-hexane as in Procedure A to obtain 1-(3-mercaptopropanoyl)-L-proline.

後処理

  1. customkept under argon at room temperature
  2. customAfter 2 hours the solvent is removed in vacuo
  3. dissolutionthe residue is dissolved in water
  4. washeluted with water
  5. customThe fractions that give
  6. concentrationconcentrated to dryness, yield 0.6 g
  7. customThis product is crystallized from ethyl acetate-hexane as in Procedure A

出典と根拠

ORDレコード
ord-c9d31e367a594153bf5fdd064fc098f3
出典データセット
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04046889

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート