Hydrochloric Acid → HCID 178443475, compound
Reaction equation
[CH3:1][C:2]([CH3:16])([CH3:15])[CH2:3][CH2:4][C:5]#[C:6][C@@H:7]1[CH2:9][C@H:8]1[C:10]1[N:11]=[CH:12][NH:13][CH:14]=1.Cl>>[CH3:1][C:2]([CH3:16])([CH3:15])[CH2:3][CH2:4]/[CH:5]=[CH:6]\[C@H:7]1[CH2:9][C@H:8]1[C:10]1[N:11]=[CH:12][NH:13][CH:14]=1Participants
3
Procedure
(1R,2R)-4-(2-(5,5-Dimethyl-cis-hex-1-enyl)cyclopropyl)imidazole was prepared by the Lindlar reduction of the compound 39 when it is trityl protected. The trityl group then deprotected after the Lindlar reduction by treating it with HCl at 90° C. for 1 h.
Sources & evidence
- ORD record
- ord-7268b9e9cd1c4fe7ac865ce83c7737ea
- Source dataset
- uspto-grants-1999_12
- Patent number
- US06008240
Reaction notes
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