4-Hydroxyphenylboronic acid → HCID 136378627, compound
Reaction equation
[C:1]1([C@H:7]([O:9][C:10](=[O:19])[NH:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][C:17]=2Cl)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:20][C:21]1[CH:26]=[CH:25][C:24](B(O)O)=[CH:23][CH:22]=1>>[C:1]1([C@H:7]([O:9][C:10](=[O:19])[NH:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][C:17]=2[C:24]2[CH:25]=[CH:26][C:21]([OH:20])=[CH:22][CH:23]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Prepared according to the procedure described in Example 1, Step 2, using the following starting materials: (4-Chloro-pyridin-3-yl)-carbamic acid (R)-1-phenyl-ethyl ester and 4-hydroxyphenylboronic acid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-1536aebd7faa4f40846fe43580120338
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09272990B2
Reaction notes
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