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p-Toluenesulfonic acid → Etoposide

HRID 64605
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HRID 64605 반응식
[CH3:1][O:2][C:3]1[C:8]([OH:9])=[C:7]([O:10][CH3:11])[CH:6]=[C:5]([C@@H:12]2[C:25]3[C:20](=[CH:21][C:22]4[O:28][CH2:27][O:26][C:23]=4[CH:24]=3)[C@@H:19]([O:29][C@@H:30]3[O:35][C@H:34]([CH2:36][OH:37])[C@@H:33]([OH:38])[C@H:32]([OH:39])[C@H:31]3[OH:40])[C@H:14]3[CH2:15][O:16][C:17](=[O:18])[C@H:13]23)[CH:4]=1.[N+](C)([O-])=O.CO[CH:47](OC)[CH3:48].C1(C)C=CC(S(O)(=O)=O)=CC=1>O.C(Cl)(Cl)Cl.CO>[CH3:47][C@H:48]1[O:38][C@H:33]2[C@H:32]([OH:39])[C@@H:31]([OH:40])[C@H:30]([O:29][C@H:19]3[C@H:14]4[CH2:15][O:16][C:17](=[O:18])[C@@H:13]4[C@H:12]([C:5]4[CH:6]=[C:7]([O:10][CH3:11])[C:8]([OH:9])=[C:3]([O:2][CH3:1])[CH:4]=4)[C:25]4[CH:24]=[C:23]5[O:26][CH2:27][O:28][C:22]5=[CH:21][C:20]3=4)[O:35][C@@H:34]2[CH2:36][O:37]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 6101p-Toluenesulfonic acidHCID 6375NitromethaneHCID 107951,1-DimethoxyethaneHCID 1599494-Demethylepipodophyllotoxin 7'-O-beta-D-glucopyranoside

생성물 1

HCID 36462Etoposide

시약·촉매·용매 3

HCID 887Methanol
용매
HCID 962Water용매
HCID 6212Chloroform용매2회

실험 절차

1.5 g. of dry 4'-demethylepipodophyllotoxin-beta-D-glucoside was suspended in 30 ml. of nitromethane, and 6 ml. of acetaldehyde-dimethylacetal and 150 mg. of p-toluene-sulphonic acid was added. The mixture was stirred at room temperature in an atmosphere of nitrogen and in the absence of moisture for one hour. After this time, the initial suspension had turned into a clear solution, and no starting material could be detected in the thin layer chromatogram (silica gel plates, eluant: chloroform+6% of methanol). Working up was effected by diluting with 400 ml. of chloroform and shaking out three times with 25 ml. each of water. The crude material obtained after concentrating the dried organic phase by evaporation was subsequently chromatographed on 100 g. of silica gel "Merck" (grain size 0.05 to 0.2 mm.), whereby chloroform containing 6% of methanol was continuously used as eluant. 4'-demethylepipodophyllotoxin-beta-D-ethylidene-glucoside, which is uniform according to thin layer chromatography, was obtained. After recrystallization from methanol colorless crystals having a M.P. of 236°-251° C., [α ]D22 =-110.5° (c.=0.588 in chloroform), were obtained.

후처리

  1. additionby diluting with 400 ml
  2. customThe crude material obtained
  3. concentrationafter concentrating the dried organic phase
  4. customby evaporation
  5. customwas subsequently chromatographed on 100 g
  6. customwas obtained
  7. customAfter recrystallization from methanol colorless crystals
  8. custom[α ]D22 =-110.5° (c.=0.588 in chloroform), were obtained

출처 및 근거

ORD 기록
ord-eb2ee955085243c680971b0331a05f57
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04609644

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