5-Hydroxy-1-indanone → HCID 178515698, compound
Reaction equation
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:8]2[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15]O)[N:10]=[CH:9]2)C=CC=CC=1.[OH:29][C:30]1[CH:31]=[C:32]2[C:36](=[CH:37][CH:38]=1)[C:35](=[O:39])[CH2:34][CH2:33]2>>[NH:8]1[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][O:29][C:30]2[CH:31]=[C:32]3[C:36](=[CH:37][CH:38]=2)[C:35](=[O:39])[CH2:34][CH2:33]3)[N:10]=[CH:9]1Participants
3
Procedure
5 mmol of 3-(1-triphenylmethyl-1H-imidazol-4-yl)propanol and 6 mmol of 5-hydroxy-1-indanone are treated as described in Example 56.
Sources & evidence
- ORD record
- ord-25d19ed06d1d4c7aa5668bcf253268d3
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248765B1
Reaction notes
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