N-(2-(p-bromophenoxy)ethyl)pyrrolidine → HCID 21182680, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]2[S:7][C:8](B(O)O)=[CH:9][C:5]=2[CH:4]=1.Br[C:16]1[CH:29]=[CH:28][C:19]([O:20][CH2:21][CH2:22][N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)=[CH:18][CH:17]=1>>[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]2[S:7][C:8]([C:16]3[CH:17]=[CH:18][C:19]([O:20][CH2:21][CH2:22][N:23]4[CH2:24][CH2:25][CH2:26][CH2:27]4)=[CH:28][CH:29]=3)=[CH:9][C:5]=2[CH:4]=1Participants
3
Procedure
The title compound was prepared in 47% yield by essentially following the procedures in Example 1, Part B, from 5-methoxybenzo[b]thiophene-2-boronic acid (Part B) and 1-(2-(4-bromophenoxy)ethyl)pyrrolidine.
Sources & evidence
- ORD record
- ord-6a5a60c62b374ebab2d13f0757e251d1
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265575B1
Reaction notes
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