5-Methylimidazo[1,2-a]pyridine → Imidazo(1,2-a)pyridine

HRID 442016Notes

Reaction equation

HRID 442016 reaction equation
Cl[C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[CH:9][N:10]=2)[CH:7]=1.C(OC1C2N(C=CN=2)C=CC=1)C1C=CC=CC=1.ClC1N2C=CN=C2C=CC=1.ClC1C=CN2C=CN=C2C=1.CC1N2C=CN=C2C=CC=1.CC1C=CC2N(C=CN=2)C=1.CC1C2N(C=CN=2)C=CC=1.C(OC1C=CC2N(C=CN=2)C=1)C1C=CC=CC=1>>[N:10]1[CH:9]=[CH:8][N:6]2[CH:7]=[CH:2][CH:3]=[CH:4][C:5]=12

Participants

9

Procedure

6-chloroimidazo[1,2-a]pyridine, 8-benzyloxyimidazo[1,2-a]pyridine, 5-chloroimidazo[1,2-a]pyridine, 7-chloroimidazo[1,2-a]pyridine, 5-methylimidazo[1,2-a]pyridine, 6-methylimidazo[1,2-a]pyridine, 8-methylimidazo[1,2-a]pyridine and 6-benzyloxyimidazo[1,2-a]pyridine.

Sources & evidence

ORD record
ord-3fa9745f0e0c4e889562bd3f552aa412
Source dataset
uspto-grants-1977_08
Patent number
US04044015

Reaction notes

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