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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(S)-4-{4-[2-(3-cyanopropylidene)hydrazino]benzyl}-1,3-oxazolidin-2-one → 3-Des[2-(Dimethylamino)ethyl] Zolmitriptan Acetonitrile

HRID 128988
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HRID 128988 반응식
C(CCC=N[NH:7][C:8]1[CH:20]=[CH:19][C:11]([CH2:12][C@H:13]2[CH2:17][O:16][C:15](=[O:18])[NH:14]2)=[CH:10][CH:9]=1)#N>C(Cl)(Cl)Cl>[C:8]([CH2:9][C:10]1[C:9]2[C:8](=[CH:20][CH:19]=[C:11]([CH2:12][C@H:13]3[CH2:17][O:16][C:15](=[O:18])[NH:14]3)[CH:10]=2)[NH:7][CH:11]=1)#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 70196055(S)-4-{4-[2-(3-cyanopropylidene)hydrazino]benzyl}-1,3-oxazolidin-2-one

생성물 1

HCID 539136153-Des[2-(Dimethylamino)ethyl] Zolmitriptan Acetonitrile수율 153.6%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of the product from step (b) (2.5 g) and polyphosphate ester (20.0 g) in chloroform (40 ml) was refluxed for 20 minutes. Ice was added to the cooled mixture and the chloroform evaporated in vacuo. The remaining aqueous phase was extracted with ethyl acetate and the combined extracts evaporated in vacuo to give the desired product as a pale yellow oil (1.8 g).

후처리

  1. additionIce was added to the cooled mixture
  2. customthe chloroform evaporated in vacuo
  3. extractionThe remaining aqueous phase was extracted with ethyl acetate
  4. customthe combined extracts evaporated in vacuo

출처 및 근거

ORD 기록
ord-e59a0d1810db42c993454408873e22ae
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05466699

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