1-Aminotetralin, (S)- → HCID 69722740, compound
Reaction equation
[CH:1]1([O:7][C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[CH:11]=O)[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.[C@@H:16]1([NH2:26])[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH2:19][CH2:18][CH2:17]1>>[CH:1]1([O:7][C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[CH2:11][NH:26][C@@H:16]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH2:19][CH2:18][CH2:17]2)[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1Participants
3
Procedure
The product from Example 59A and (1S)-1,2,3,4-tetrahydro-1-naphthalenylamine were processed as described in Example 1A to provide the title compound.
Sources & evidence
- ORD record
- ord-762f203d99284e7887c36daf148e2796
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831193B2
Reaction notes
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