Pyrrolidine → 1-[4-(3,5-Dichloro-phenoxy)-benzyl]-pyrrolidine
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([Cl:17])[CH:16]=1)[O:5][C:6]1[CH:13]=[CH:12][C:9]([CH:10]=O)=[CH:8][CH:7]=1.[NH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([Cl:17])[CH:16]=1)[O:5][C:6]1[CH:13]=[CH:12][C:9]([CH2:10][N:18]2[CH2:22][CH2:21][CH2:20][CH2:19]2)=[CH:8][CH:7]=1Participants
3
Procedure
The title compound was prepared starting from 4-(3,5-dichloro-phenoxy)-benzaldehyde and pyrrolidine by the same method (step B) described in Example 1. 1H NMR (400 MHz, CDCI3)δ7.22 (t, J=7.8 Hz, 1 H), 7.07 (d, J=7.6 Hz,1 H), 6.96 (m, 2 H), 6.81 (m,1 H), 6.76 (m, 2 H), 3.52 (s, 2 H), 2.45 (m, 4 H), 1.70 (m, 4 H).
Sources & evidence
- ORD record
- ord-8be90798025a4f9eb3529acf116cd19b
- Source dataset
- uspto-grants-2003_10
- Patent number
- US06638967B2
Reaction notes
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