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Indole → 3-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)-1H-indole hydroiodide

HRID 1075786
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반응식

HRID 1075786 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[NH:10]1[CH2:14][CH2:13][NH:12][C:11]1=[S:15].[I:16]I.[I-].[K+]>CO.O>[IH:16].[NH:12]1[CH2:13][CH2:14][N:10]=[C:11]1[S:15][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 798IndoleHCID 807IodineHCID 4875Potassium IodideHCID 2723650Ethylenethiourea

생성물 1

HCID 867333733-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)-1H-indole hydroiodide

시약·촉매·용매 2

HCID 887Methanol용매2회
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 962
Water
용매

실험 절차

A mixture of 11.7 g indole in 100 ml methanol and 10.2 g 2-imidazolidinethione in 150 ml methanol is added to a well-stirred solution of 25.4 g iodine and 50 g potassium iodide in 100 ml water. The mixture is stirred for 2 hours at room temperature. The clear solution is concentrated in vacuo to one third of the original volume and cooled. The solid which separates is filtered off, dried and recrystallised from alcohol-ether to give 3-(2-imidazolin-2-ylthio)-indole hydriodide of the formula ##SPC9##

후처리

  1. concentrationThe clear solution is concentrated in vacuo to one third of the original volume
  2. temperaturecooled
  3. filtrationThe solid which separates is filtered off
  4. customdried
  5. customrecrystallised from alcohol-ether

출처 및 근거

ORD 기록
ord-916e7c9e10e5428fbf74d51277c5e34f
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03954757

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