6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone → HCID 178515874, 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:37](=[CH:38][CH:39]=1)[C:36](=[O:40])[CH2:35][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:37](=[CH:38][CH:39]=2)[C:36](=[O:40])[CH2:35][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 3,4-dihydro-6-hydroxy-2H-naphthalen-1-one are treated as described in Example 56.
Sources & evidence
- ORD record
- ord-a2b8e86ceca241dda1a2fce547f9822d
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248765B1
Reaction notes
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