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Pyridine → HCID 14954045, 화합물

HRID 863666
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HRID 863666 반응식
[C:1]([O:4][C:5](=O)C)(=[O:3])[CH3:2].[NH:8]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]3N=CC=C[C:15]3=2)[CH:10]=[CH:9]1.N1[CH:26]=[CH:25][CH:24]=[CH:23]C=1>>[C:1]([O:4][CH2:5][CH:25]1[CH2:24][CH2:23][N:8]2[C:16]3[C:11]([CH:10]=[C:9]2[CH2:26]1)=[CH:12][CH:13]=[CH:14][CH:15]=3)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 178420737HCID 178420737, 화합물

생성물 1

HCID 14954045HCID 14954045, 화합물

실험 절차

11.4 g of acetic anhydride were added to a solution of 11.0 g of the pyridoindole from c) in 100 ml of pyridine and the resulting solution was stirred under a nitrogen atmosphere for 18 hours. The majority of the pyridine was removed by evaporation and the residue was acidified with 2M hydrochloric acid. The mixture was extracted with diethyl ether and the combined extracts were washed with sodium bicarbonate solution and with water. The extracts were dried and evaporated to dryness to give 11.25 g of 8-(acetoxymethyl)-6,7,8,9-tetrahydropyrido[1,2-a]indole of melting point 63°-64° C.

후처리

  1. customThe majority of the pyridine was removed by evaporation
  • extractionThe mixture was extracted with diethyl ether
  • washthe combined extracts were washed with sodium bicarbonate solution and with water
  • customThe extracts were dried
  • customevaporated to dryness
  • 출처 및 근거

    ORD 기록
    ord-265e4f2d58d443ff8bb53526f0411de6
    출처 데이터셋
    uspto-grants-1998_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05721245

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