Thiophene-3-methanol → HCID 53951305, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([NH:11][C@H:12]([C:14]([OH:16])=[O:15])[CH3:13])=[O:10])[CH:5]=[CH:6][CH:7]=1.[S:17]1[CH:21]=[CH:20][C:19]([CH2:22]O)=[CH:18]1>>[S:17]1[CH:21]=[CH:20][C:19]([CH2:22][O:15][C:14](=[O:16])[C@H:12]([CH3:13])[NH:11][C:9](=[O:10])[CH2:8][C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=2)=[CH:18]1Participants
3
Procedure
Following General Procedure C above, and using N-(3-chlorophenylacetyl alanine (from Example D above) and 3-thiophenemethanol (Aldrich) the title compound can be prepared. The reaction was monitored by tlc on silica gel and purification was by liquid chromatography using 3:7 EtOAc:hexane as the eluant.
Sources & evidence
- ORD record
- ord-8ef06837c40f48b3877059589874a079
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06117901
Reaction notes
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