HCID 11241897, compound → 3-(5-Bromo-2,3,3-trimethyl-3H-pyrrolo[2,3-b]pyridin-7-ium-7-yl)propane-1-sulfonate
Reaction equation
Cl[C:2]1[CH:3]=[C:4]2[C:17]([CH3:19])([CH3:18])[C:16]([CH3:20])=[N:15][C:5]2=[N+:6]([CH2:8][CH2:9][CH2:10][S:11]([O-:14])(=[O:13])=[O:12])[CH:7]=1.[Br:21]C1C=C2C(C)(C)C(C)=NC2=NC=1>>[Br:21][C:2]1[CH:3]=[C:4]2[C:17]([CH3:19])([CH3:18])[C:16]([CH3:20])=[N:15][C:5]2=[N+:6]([CH2:8][CH2:9][CH2:10][S:11]([O-:14])(=[O:13])=[O:12])[CH:7]=1Participants
3
Procedure
Compound 6 was prepared analogously to compound 5 (Example 5), except that 5-bromo-2,3,3-trimethyl-3H-pyrrolo[2,3-b]pyridine (50) was used as a starting material.
Sources & evidence
- ORD record
- ord-7d2dd0a1c0704f79863ad43da0c7ea18
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927719B2
Reaction notes
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