2-Bromomethyl-3-iodo-pyridine → N-(3-iodo-pyridin-2-ylmethyl)-N-(2-vinyl-phenyl)-acetamide
Reaction equation
Br[CH2:2][C:3]1[C:8]([I:9])=[CH:7][CH:6]=[CH:5][N:4]=1.ClC1C(C[N:18]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[CH:28]=[CH2:29])[C:19](=[O:21])[CH3:20])=CC(F)=C(Cl)N=1>>[I:9][C:8]1[C:3]([CH2:2][N:18]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[CH:28]=[CH2:29])[C:19](=[O:21])[CH3:20])=[N:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Compound 51C (8.5 mg, 70%) was prepared from bb (5.2 mg, 0.032 mmol) and 51B (9.7 mg, 0.33 mmol) by a route analogous to that used for the preparation of 1C. HPLC Rt=2.929 min.
Sources & evidence
- ORD record
- ord-955308d3ac7e499c886f64a99202ad61
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378426B2
Reaction notes
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