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Sodium Hydroxide → 3-Demethylthiocolchicine

HRID 2308993
ノート
印刷プレビュー

反応式

HRID 2308993 の反応式
[CH3:1][C:2]([NH:4][CH:5]1[C:21]2[C:14](=[CH:15][CH:16]=[C:17]([S:22][CH3:23])[C:18]([CH:20]=2)=[O:19])[C:13]2[C:12]([O:24][CH3:25])=[C:11]([O:26][CH3:27])[C:10]([O:28][C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=[CH:9][C:8]=2[CH2:7][CH2:6]1)=[O:3].[OH-].[Na+]>P(=O)(O)(O)O.CO>[CH3:1][C:2]([NH:4][C@@H:5]1[C:21]2[C:14](=[CH:15][CH:16]=[C:17]([S:22][CH3:23])[C:18]([CH:20]=2)=[O:19])[C:13]2[C:8](=[CH:9][C:10]([OH:28])=[C:11]([O:26][CH3:27])[C:12]=2[O:24][CH3:25])[CH2:7][CH2:6]1)=[O:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 72067N-[1,2-dimethoxy-10-methylsulfanyl-9-oxo-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide2 回

生成物 1

HCID 840763-Demethylthiocolchicine収率 94.3%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 1004
Phosphoric Acid
溶媒

実験手順

A solution of thiocolchicoside (2.3 g, 3.96 mmol) in phosphoric acid (85-88%, 65 ml) after dissolving by heating, was stirred at room temperature for overnight. The TLC analysis showed the absence of thiocolchicoside in the reaction mixture, (one small drop of reaction mixture was diluted with MeOH (0.5 ml) and applied to a TLC plate and run in solvent system A). The reaction mixture was poured on ice, adjusted to pH 5 by the addition of 15% aqueous NaOH solution, followed by several extractions with CH2Cl2 (4×25 ml). The combined organic layers were dried (Na2SO4) and evaporated to afford a residue, which was crystallized with acetone to afford 3-demethylthiocolchicine as a yellow solid (1.5 g, 93%), mp 316° C.; [α]D25 =-251° (c 0.21, CHCl3); IR (CHCl3) cm-1 ; 3440 (OH); CIMS: m/e 402 (M+ +1); Anal. Calcd. for C21H23NO5S: C, 62.82; H, 5.77; N, 3.48; S, 7.98. Found C, 63.09; H, 5.86; N, 3.26; S, 8.25%.

後処理

  1. temperatureby heating
  2. custom(one small drop of reaction mixture
  3. additionThe reaction mixture was poured on ice
  4. extractionfollowed by several extractions with CH2Cl2 (4×25 ml)
  5. dry with materialThe combined organic layers were dried (Na2SO4)
  6. customevaporated
  7. customto afford a residue, which
  8. customwas crystallized with acetone

出典と根拠

ORDレコード
ord-8df3cf768a864b6e8908d14f76e524e0
出典データセット
uspto-grants-1987_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04692463

反応ノート

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