HCID 11241897, compound → 3-(5-Bromo-2,3,3-trimethyl-3H-pyrrolo[2,3-b]pyridin-7-ium-7-yl)propane-1-sulfonate

HRID 1480505Notes

Reaction equation

HRID 1480505 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]=1

Participants

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-55dedefe0c7d4b5d80c083a34b89777b
Source dataset
uspto-grants-2016_08
Patent number
US09408924B2

Reaction notes

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