1,1'-Carbonyldiimidazole → HCID 59394510, compound

HRID 45115

Reaction equation

HRID 45115 reaction equation
[CH2:1]([O:8][CH2:9][C:10]1[N:15]=[CH:14][N:13]=[C:12]([O:16][C:17]2[CH:18]=[C:19]3[C:23](=[CH:24][CH:25]=2)[NH:22][CH:21]=[CH:20]3)[CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1N=CN([C:31]([N:33]2C=N[CH:35]=[CH:34]2)=[O:32])C=1.[CH3:38][O:39][C:40]1[CH:46]=CC(N)=[CH:42][C:41]=1[C:47]([F:50])([F:49])[F:48]>ClCCCl.C(Cl)Cl>[CH2:1]([O:8][CH2:9][C:10]1[N:15]=[CH:14][N:13]=[C:12]([O:16][C:17]2[CH:18]=[C:19]3[C:23](=[CH:24][CH:25]=2)[N:22]([C:31]([NH:33][C:34]2[CH:35]=[CH:46][C:40]([O:39][CH3:38])=[C:41]([C:47]([F:50])([F:49])[F:48])[CH:42]=2)=[O:32])[CH:21]=[CH:20]3)[CH:11]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

To a solution of 5-(6-(benzyloxymethyl)pyrimidin-4-yloxy)-1H-indole (0.8 g, 2.41 mmol) in 35 mL of DCE, CDI (1.17 g, 7.24 mmol) is added followed by TEA (1 mL, 7.24 mmol). Mixture is stirred at rt overnight and then 4-methoxy-3-(trifluoromethyl)aniline (1.38 g, 7.24 mmol) is added followed by stirring for 4 days. The reaction is diluted with DCM, washed with saturated aqueous NaHCO3 (×2), brine, and the organic layer is dried over Na2SO4. After concentration, the residue is purified by FCC (5-60% EtOAc/heptane) to give the title compound. MS (ESI) m/z 549.1 (M+1).

Workup

  1. stirringby stirring for 4 days
  2. washwashed with saturated aqueous NaHCO3 (×2), brine
  3. dry with materialthe organic layer is dried over Na2SO4
  4. concentrationAfter concentration
  5. customthe residue is purified by FCC (5-60% EtOAc/heptane)

Sources & evidence

ORD record
ord-5f07ad80665e4cda83646908f72ce0a4
Source dataset
uspto-grants-2013_09
Patent number
US08541432B2

Linked notes

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