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Dichloromethane → HCID 66764117, 화합물

HRID 510169
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HRID 510169 반응식
[CH:1]([S:4]([C:7]1[CH:12]=[CH:11][C:10]([C:13]2[N:14]=[C:15]3[CH:21]=[CH:20][NH:19][C:16]3=[N:17][CH:18]=2)=[CH:9][CH:8]=1)(=[O:6])=[O:5])([CH3:3])[CH3:2].[I:22]Cl.ClCCl.CCOC(C)=O>N1C=CC=CC=1>[I:22][C:21]1[C:15]2[C:16](=[N:17][CH:18]=[C:13]([C:10]3[CH:9]=[CH:8][C:7]([S:4]([CH:1]([CH3:3])[CH3:2])(=[O:6])=[O:5])=[CH:12][CH:11]=3)[N:14]=2)[NH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 8857Ethyl AcetateHCID 24640Iodine chlorideHCID 667640832-(4-isopropylsulfonylphenyl)-5H-pyrrolo[2,3-b]pyrazine

생성물 1

HCID 66764117HCID 66764117, 화합물수율 46.79%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To 2-(4-isopropylsulfonylphenyl)-5H-pyrrolo[2,3-b]pyrazine (9 g, 29.86 mmol) in pyridine (90.00 mL) at RT was added a 1M solution of iodine monochloride in dichloromethane (32.85 mL of 1 M, 32.85 mmol). The resulting dark brown solution was stirred at RT for 4 hours then taken into EtOAc and washed with aqueous sodium thiosulphate/NaHCO3×2 then with brine, then dried over MgSO4 and concentrated under reduced pressure. The solid residue was triturated with acetonitrile, filtered and washed with acetonitrile, dried in vacuo to give the subtitle compound (5.97 g, 13.97 mmol, 46.79%). 1H NMR (400.0 MHz, DMSO) δ 12.72 (s, 1H), 9.03 (s, 1H), 8.46 (d, J=8.5 Hz, 2H), 8.23 (s, 1H), 8.01 (d, J=8.5 Hz, 2H), 3.49 (t, J=6.8 Hz, 1H) and 1.20 (d, J=6.8 Hz, 6H) ppm; MS (ES+) 428.0.

후처리

  1. washwashed with aqueous sodium thiosulphate/NaHCO3×2
  2. dry with materialwith brine, then dried over MgSO4
  3. concentrationconcentrated under reduced pressure
  4. customThe solid residue was triturated with acetonitrile
  5. filtrationfiltered
  6. washwashed with acetonitrile
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-52fbf83a33ea45c1a2ef98f073b09f33
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096602B2

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