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Diiodomethane → 2-Amino-5-[4-(difluoromethoxy)phenyl]-5-{3-[2-(methoxymethyl)-cyclopropyl]phenyl}-3-methyl-3,5-dihydro-4H-imidazol-4-one

HRID 30586
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HRID 30586 반응식
[CH2:1]([Zn]CC)C.C(C(O)=O)(F)(F)F.C(I)I.[NH2:16][C:17]1[N:21]([CH3:22])[C:20](=[O:23])[C:19]([C:35]2[CH:40]=[CH:39][C:38]([O:41][CH:42]([F:44])[F:43])=[CH:37][CH:36]=2)([C:24]2[CH:29]=[CH:28][CH:27]=[C:26](/[CH:30]=[CH:31]/[CH2:32][O:33][CH3:34])[CH:25]=2)[N:18]=1>C(Cl)Cl>[NH2:16][C:17]1[N:21]([CH3:22])[C:20](=[O:23])[C:19]([C:35]2[CH:36]=[CH:37][C:38]([O:41][CH:42]([F:44])[F:43])=[CH:39][CH:40]=2)([C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([CH:30]3[CH2:1][CH:31]3[CH2:32][O:33][CH3:34])[CH:25]=2)[N:18]=1
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참가 물질

6

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HCID 6346DiiodomethaneHCID 6422Trifluoroacetic acidHCID 161145862-amino-5-[4-(difluoromethoxy)phenyl]-5-{3-[(1E)-3-methoxyprop-1-en-1-yl]phenyl}-3-methyl-3,5-dihydro-4H-imidazol-4-oneHCID 178418750HCID 178418750, 화합물

생성물 1

HCID 161145842-Amino-5-[4-(difluoromethoxy)phenyl]-5-{3-[2-(methoxymethyl)-cyclopropyl]phenyl}-3-methyl-3,5-dihydro-4H-imidazol-4-one수율 16%

시약·촉매·용매 1

HCID 6344Dichloromethane용매4회

실험 절차

A 1M solution of diethyl zinc (4.92 ml, 4.92 mmol) in dry CH2Cl2 at 0° C. is treated very slowly with a solution of CF3CO2H (0.56 g, 4.92 mmol) in dry CH2Cl2, stirred for 20 min, treated dropwise with a solution of CH2I2 (0.66 g, 2.46 mmol) in dry CH2Cl2, stirred for 20 min, treated with a solution of 2-amino-5-[4-(difluoromethoxy)phenyl]-5-{3-[(1E)-3-methoxyprop-1-en-1-yl]phenyl}-3-methyl-3,5-dihydro-4H-imidazol-4-one (197 mg, 0.492 mmol) in dry CH2Cl2, allowed to come to room temperature, stirred for 2 h at room temperature, quenched with aqueous NH4Cl and extracted with CH2Cl2. The combined extracts are dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by SCX cartridge and preparative HPLC to give the title compound as a white solid, 32 mg (16% yield), identified by NMR and mass spectral analyses. (1H-NMR 300 MHz, DMSO): 7.46(d, 2H); 7.24-7.13(m, 3H); 7.16(t, 1H); 7.10(d, 2H); 6.88(m, 1H); 6.64(s br, 2H); 3.44-3.34(m, 2H); 3.24(m, 1H); 3.23(s, 3H); 2.97(s, 3H); 1.76(m, 1H); 0.90-0.76(m, 2H). MS [M+H]+ 416.1

후처리

  1. stirringstirred for 20 min
  2. customto come to room temperature
  3. stirringstirred for 2 h at room temperature
  4. customquenched with aqueous NH4Cl
  5. extractionextracted with CH2Cl2
  6. dry with materialThe combined extracts are dried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customThe resultant residue is purified by SCX cartridge and preparative HPLC

출처 및 근거

ORD 기록
ord-a0c17451ec69485d91300d7732655d82
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07423158B2

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