Thiophene, 2,3-dichloro- → HCID 58017207, compound
Reaction equation
[Cl:1][C:2]1[S:3][CH:4]=[CH:5][C:6]=1[Cl:7].[C:8]([O:12][C:13]([N:15]1[CH2:19][CH2:18][C:17]([CH:23]=[O:24])([CH2:20][CH2:21][CH3:22])[CH2:16]1)=[O:14])([CH3:11])([CH3:10])[CH3:9]>>[C:8]([O:12][C:13]([N:15]1[CH2:19][CH2:18][C:17]([CH:23]([C:4]2[S:3][C:2]([Cl:1])=[C:6]([Cl:7])[CH:5]=2)[OH:24])([CH2:20][CH2:21][CH3:22])[CH2:16]1)=[O:14])([CH3:10])([CH3:11])[CH3:9]Participants
3
Procedure
3-[(4,5-Dichloro-thiophen-2-yl)-hydroxy-methyl]-3-propyl-pyrrolidine-1-carboxylic acid tert-butyl ester was prepared from 2,3-dichloro-thiophene and 3-formyl-3-propyl-pyrrolidine-1-carboxylic acid tert-butyl ester using the procedure of step 1 of Example 20.
Sources & evidence
- ORD record
- ord-1338fbdece2e4e41894fb7380f11522d
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513425B2
Reaction notes
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