Methanesulfonic Acid → HCID 178498219, compound

HRID 542534Notes

Reaction equation

HRID 542534 reaction equation
[CH3:1][N:2]([CH3:29])[CH2:3][CH2:4][N:5]=[CH:6][C:7]1[C:20]([OH:21])=[C:19]([CH3:22])[C:18]([OH:23])=[C:17]2[C:8]=1[N:9]=[C:10]1[C:15](=[N:16]2)[C:14]([C:24]([O:26][CH3:27])=[O:25])=[CH:13][CH:12]=[C:11]1[OH:28].[CH3:30][S:31]([OH:34])(=[O:33])=[O:32]>O>[CH3:30][S:31]([OH:34])(=[O:33])=[O:32].[CH3:29][N:2]([CH3:1])[CH2:3][CH2:4][N:5]=[CH:6][C:7]1[C:20]([OH:21])=[C:19]([CH3:22])[C:18]([OH:23])=[C:17]2[C:8]=1[N:9]=[C:10]1[C:15](=[N:16]2)[C:14]([C:24]([O:26][CH3:27])=[O:25])=[CH:13][CH:12]=[C:11]1[OH:28]

Participants

4

Procedure

6-[[[2-(Dimethylamino)ethyl]imino]methyl]-4,7,9-trihydroxy-8-methyl-1-phenazinecarboxylic acid, methyl ester (468 mg, 1.177 mmol) was stirred at room temperature with methanesulfonic acid (125 mg, 1.3 mmol) in 20 ml of water until dissolution was complete.

Sources & evidence

ORD record
ord-73223dc0855e47b8b0c64b87615bad7e
Source dataset
uspto-grants-1987_04
Patent number
US04657909

Reaction notes

Loading…