HCID 15839397, compound → HCID 18918740, compound
Reaction equation
[CH:1]1([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][N:14]([C:17]3[C:25]([O:26][CH3:27])=[CH:24][C:20]4[CH2:21][CH2:22][O:23][C:19]=4[CH:18]=3)[CH2:13][CH2:12]2)[C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=2[CH2:2]1.S(O[CH2:33][CH2:34][C:35]1C2CCCCCC=2C=CC=1)(=O)(=O)C>>[C:1]1([CH2:9][CH2:10][N:11]2[CH2:12][CH2:13][N:14]([C:17]3[C:25]([O:26][CH3:27])=[CH:24][C:20]4[CH2:21][CH2:22][O:23][C:19]=4[CH:18]=3)[CH2:15][CH2:16]2)[C:2]2[CH2:33][CH2:34][CH2:35][CH2:7][CH2:8][C:3]=2[CH:6]=[CH:5][CH:4]=1Participants
3
Procedure
Prepared in the same manner as the product of Example 3 but using 2-(benzocycloheptan-1-yl)ethanol mesylate instead of 2-(benzocyclobutan-1-yl)-1-bromoethane.
Sources & evidence
- ORD record
- ord-7a5bf0a30f864de7af0aead887bd5c42
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05684020
Reaction notes
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