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N-Iodosuccinimide → HCID 69478504, 화합물

HRID 1183203
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HRID 1183203 반응식
[F:1][CH2:2][CH2:3][N:4]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][C:12]([C@H:15]3[CH2:17][C@@H:16]3[C:18]([O:20][CH2:21][CH3:22])=[O:19])=[CH:11][CH:10]=2)[N:6]=[CH:5]1.[I:23]N1C(=O)CCC1=O.C(=O)(O)[O-].[Na+]>ClCCl.FC(F)(F)C(O)=O>[F:1][CH2:2][CH2:3][N:4]1[C:8]([I:23])=[C:7]([C:9]2[CH:14]=[CH:13][C:12]([C@H:15]3[CH2:17][C@@H:16]3[C:18]([O:20][CH2:21][CH3:22])=[O:19])=[CH:11][CH:10]=2)[N:6]=[CH:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 120273N-IodosuccinimideHCID 516892Sodium BicarbonateHCID 86664898HCID 86664898, 화합물

생성물 1

HCID 69478504HCID 69478504, 화합물수율 17.3%

시약·촉매·용매 2

HCID 6422Trifluoroacetic acid촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of ethyl (1S,2S)-2-{4-[1-(2-fluoroethyl)-1H-imidazol-4-yl]phenyl}cyclopropanecarboxylate (450 mg, 1.488 mmol) in dichloromethane (5 mL) was added N-iodosuccinimide (352 mg, 1.563 mmol) and three drops trifluoroacetic acid. The reaction was stirred at rt for 3 h. The mixture was neutralized with aqueous sodium bicarbonate and the organics were extracted with dichloromethane. The organics were then washed with aqueous sodium thiosulfate, followed by three washes with water. The organics were dried (MgSO4), concentrated, and purified on 20 g of silica gel eluting a gradient of 35-100% ethyl acetate in hexanes to give rise to the title compound as a brown oil (110 mg, 0.257 mmol). LCMS: [M+1]+=429.

후처리

  1. extractionthe organics were extracted with dichloromethane
  2. washThe organics were then washed with aqueous sodium thiosulfate
  3. dry with materialThe organics were dried (MgSO4)
  4. concentrationconcentrated
  5. custompurified on 20 g of silica gel eluting a gradient of 35-100% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-d38cf30e76554b9f8ac7bce9d14cdf6d
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664253B2

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