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Acetic Acid → 2,3-Dihydro-1'-methylspiro[furo[2,3-f]indole-3,4'-piperidine]

HRID 1741034
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HRID 1741034 반응식
[C:1]([CH2:3][C:4]1[C:9]([N+:10]([O-])=O)=[CH:8][C:7]2[C:13]3([CH2:20][O:21][C:6]=2[CH:5]=1)[CH2:18][CH2:17][N:16]([CH3:19])[CH2:15][CH2:14]3)#N.O.C(O)(=O)C>[Pd].C(O)C>[CH3:19][N:16]1[CH2:17][CH2:18][C:13]2([C:7]3[CH2:8][C:9]4[C:4]([CH:3]=[CH:1][N:10]=4)=[CH:5][C:6]=3[O:21][CH2:20]2)[CH2:14][CH2:15]1
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참가 물질

6

반응물 3

HCID 176Acetic AcidHCID 962WaterHCID 186900676-(Cyanomethyl)-2,3-dihydro-1'-methyl-5-nitrospiro[benzofuran-3,4'-piperidine]

생성물 1

HCID 701980042,3-Dihydro-1'-methylspiro[furo[2,3-f]indole-3,4'-piperidine]수율 10%

시약·촉매·용매 2

HCID 23938Palladium촉매
HCID 702
Ethanol
용매

실험 절차

6-(Cyanomethyl)-2,3-dihydro-1'-methyl-5-nitrospiro[benzofuran-3,4'-piperidine] (D6, 0.35 g, 1.2 mmol) was hydrogenated at 50 psiH2 over 10% palladium on charcoal (0.30 g) in a mixture of ethanol (18 ml), water (2 ml) and acetic acid (0.15 ml) for 24 h. Catalyst was filtered off onto kieselguhr, and the filtrate was evaporated to dryness. Chromatography on silica gel, eluting with 0-12% methanol/chloroform (gradient) gave the title compound (0.020 g, 10%) as a pale orange solid.

후처리

  1. filtrationCatalyst was filtered off onto kieselguhr
  2. customthe filtrate was evaporated to dryness
  3. washChromatography on silica gel, eluting with 0-12% methanol/chloroform (gradient)

출처 및 근거

ORD 기록
ord-816466d8edf8447586ccbe183944ff26
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05972951

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