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Iodine → 3-iodo-5-(6-isopropoxypyrazin-2-yl)-1H-indole

HRID 1529309
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반응식

HRID 1529309 반응식
[CH:1]([O:4][C:5]1[N:10]=[C:9]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][CH:15]=[CH:14]3)[CH:8]=[N:7][CH:6]=1)([CH3:3])[CH3:2].[OH-].[K+].[I:22]I>CN(C=O)C>[I:22][C:14]1[C:13]2[C:17](=[CH:18][CH:19]=[C:11]([C:9]3[CH:8]=[N:7][CH:6]=[C:5]([O:4][CH:1]([CH3:3])[CH3:2])[N:10]=3)[CH:12]=2)[NH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 807Iodine2회HCID 14797Potassium HydroxideHCID 679597185-(6-propan-2-yloxypyrazin-2-yl)-1H-indole

생성물 1

HCID 679599583-iodo-5-(6-isopropoxypyrazin-2-yl)-1H-indole수율 102.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 5-(6-isopropoxy-pyrazin-2-yl)-1H-indole (32 g, 0.126 mol) in DMF (250 mL) was added KOH (17.8 g, 0.316 mol) and then stirred for 15 min at RT. I2 (35.3 g, 0.139 mol) was added to the reaction mixture and stirred at RT for another 1 h. Then reaction mixture was poured into ice water and excess of I2 was quenched with sodium thiosulfite. The resulting solid was collected by filtration, washed with water and dried under vacuum to afford crude 3-iodo-5-(6-isopropoxypyrazin-2-yl)-1H-indole (49 g) as pale brown solid. MS (ESI, m/z): 379.9 (M+1). This material was used to further step without purification.

후처리

  1. stirringstirred at RT for another 1 h
  2. customThen reaction mixture
  3. customwas quenched with sodium thiosulfite
  4. filtrationThe resulting solid was collected by filtration
  5. washwashed with water
  6. customdried under vacuum

출처 및 근거

ORD 기록
ord-548cb172099348ad950af735bdcd369c
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09090593B2

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