(3S)-1-(2-Phenylethyl)-3-pyrrolidinamine → HCID 59915938, compound
Reaction equation
[C:1]12([S:11](Cl)(=[O:13])=[O:12])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[NH2:15][C@H:16]1[CH2:20][CH2:19][N:18]([CH2:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:17]1>>[C:23]1([CH2:22][CH2:21][N:18]2[CH2:19][CH2:20][C@H:16]([NH:15][S:11]([C:1]34[CH2:10][CH:5]5[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]5)[CH2:2]3)[CH2:8]4)(=[O:13])=[O:12])[CH2:17]2)[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1Participants
3
Procedure
1-Adamantanesulfonyl chloride and (S)-3-amino-1-(2-phenylethyl)pyrrolidine were reacted under the same conditions as in Example 53 to give (S)-N-(1-(2-phenylethyl)pyrrolidin-3-yl)-1-adamantanesulfonamide.
Sources & evidence
- ORD record
- ord-c6b4f9843e8d448596e597eb2a309082
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06468998B1
Reaction notes
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