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Sodium Hydroxide → 3-Demethylthiocolchicine

HRID 2308993
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HRID 2308993 반응식
[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]
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참가 물질

5

반응물 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]acetamide2회

생성물 1

HCID 840763-Demethylthiocolchicine수율 94.3%

시약·촉매·용매 2

HCID 887Methanol용매
HCID 1004
Phosphoric Acid
용매

실험 절차

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%.

후처리

  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

출처 및 근거

ORD 기록
ord-8df3cf768a864b6e8908d14f76e524e0
출처 데이터셋
uspto-grants-1987_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04692463

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