1-Iodopropane → HCID 118557854, compound
Reaction equation
[C:1]([C:4]1[CH:5]=[N:6][CH:7]=[CH:8][C:9]=1[CH2:10][CH:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([O:21][CH3:22])[CH:17]=2)[C:12]1=[O:23])(=[O:3])[CH3:2].[CH2:24]([I:27])[CH2:25][CH3:26]>>[I-:27].[C:1]([C:4]1[CH:5]=[N+:6]([CH2:24][CH2:25][CH3:26])[CH:7]=[CH:8][C:9]=1[CH2:10][CH:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([O:21][CH3:22])[CH:17]=2)[C:12]1=[O:23])(=[O:3])[CH3:2]Participants
3
Procedure
The title compound 135 is prepared according to the procedure reported in Example 38.1 with compound 103 (100.0 mg, 0.323 mmol) and propyl iodide (63 μL, 2 equiv) as reactants. Yellow solid. (Yield 116.2 mg, 75%).
Sources & evidence
- ORD record
- ord-dff7849526784ca4b49390903b4f1e0d
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376387B2
Reaction notes
Loading…