Tert-butyl 4-iodo-6-phenylpyridin-3-ylcarbamate → (4'-Iodo-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-5'-yl)carbamic acid tert-butyl ester
Reaction equation
[C:1]([O:5][C:6](=[O:20])[NH:7][C:8]1[CH:9]=[CH:10][C:11]([N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)=[N:12][CH:13]=1)([CH3:4])([CH3:3])[CH3:2].C(OC(=O)NC1C=NC(C2C=CC=CC=2)=CC=1[I:34])(C)(C)C>>[C:1]([O:5][C:6](=[O:20])[NH:7][C:8]1[C:9]([I:34])=[CH:10][C:11]([N:14]2[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]2)=[N:12][CH:13]=1)([CH3:4])([CH3:2])[CH3:3]Participants
3
Procedure
The title product was prepared from (3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-yl)carbamic acid tert-butyl ester in the same manner as described in the preparation of (4-iodo-6-phenylpyridin-3-yl)carbamic acid tert-butyl ester.
Sources & evidence
- ORD record
- ord-fcbc2bc451174145b9c401df778fc444
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08741897B2
Reaction notes
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