2-Chlorophenylboronic acid → HCID 86670731, compound
Reaction equation
[C:1]([O:5][C:6](=[O:18])[N:7]([CH2:15][CH2:16][F:17])[C:8]1[CH:9]=[N:10][CH:11]=[CH:12][C:13]=1I)([CH3:4])([CH3:3])[CH3:2].[Cl:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1B(O)O>>[C:1]([O:5][C:6](=[O:18])[N:7]([C:8]1[CH:9]=[N:10][CH:11]=[CH:12][C:13]=1[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=1[Cl:19])[CH2:15][CH2:16][F:17])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared in analogy to example 72, from (2-fluoro-ethyl)-(4-iodo-pyridin-3-yl)-carbamic acid tert-butyl ester and 2-chlorophenylboronic acid (CAS RN 1679-18-1). Yellow oil (86%). MS (ESI): m/z=351.13 [M+H]+.
Sources & evidence
- ORD record
- ord-29d6058a6a5b4149bb04c0b7c88be80a
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987307B2
Reaction notes
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