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3-(4-Pyridyl)-2,3,3a,4,5,6-hexahydrobenzo[6,7]cyclohepta[1,2-c] pyrazole → HCID 178419887, 화합물

HRID 1580159
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HRID 1580159 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH:7]2[NH:11][N:10]=[C:9]3[C:12]4[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=4[CH2:14][CH2:15][CH2:16][CH:8]23)=[CH:3][CH:2]=1>[O-2].[O-2].[Mn+4].C1C=CC=CC=1>[N:1]1[CH:2]=[CH:3][C:4]([C:7]2[NH:11][N:10]=[C:9]3[C:12]4[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=4[CH2:14][CH2:15][CH2:16][C:8]=23)=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 215649633-(4-Pyridyl)-2,3,3a,4,5,6-hexahydrobenzo[6,7]cyclohepta[1,2-c] pyrazole

생성물 1

HCID 178419887HCID 178419887, 화합물

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 241Benzene용매

실험 절차

Into a flask eqipped with a magnetic stirring bar is charged 5.0 grams of 3-(4-pyridyl)-2,3,3a,4,5,6-hexahydrobenzo[6,7]cyclohepta[1,2-c] pyrazole, 25 grams of activated manganese dioxide and 150 ml of dry benzene. The mixture is stirred for about 12 hours at room temperature, after which the manganese salts are filtered off and the solvent removed in vacuo. The solid is crystallized from ethanol to give 3-(4-pyridyl)-2,4,5,6-tetrahydrobenzo[ 6,7]cyclohepta[1,2-c]pyrazole (m.p. 217°-219°C).

후처리

  1. customInto a flask eqipped with a magnetic stirring bar
  2. filtrationafter which the manganese salts are filtered off
  3. customthe solvent removed in vacuo
  4. customThe solid is crystallized from ethanol

출처 및 근거

ORD 기록
ord-46eddc267fac4966a2ddfacf8695e3f6
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03932430

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