Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 59436141, compound

HRID 1624690Notes

Reaction equation

HRID 1624690 reaction equation
Cl.[CH3:2][O:3][C:4]1[C:5](=[O:19])[C:6]([C:16]([OH:18])=O)=[N:7][N:8]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:9]=1.Cl.[CH3:21][NH:22][O:23][CH3:24].F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1>CN(C=O)C.CCOC(C)=O>[CH3:24][O:23][N:22]([CH3:21])[C:16]([C:6]1[C:5](=[O:19])[C:4]([O:3][CH3:2])=[CH:9][N:8]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[N:7]=1)=[O:18]

Participants

6

Procedure

A mixture of 5-methoxy-4-oxo-1-pyridin-3-yl-1,4-dihydropyridazine-3-carboxylic acid hydrochloride (1.0 g, 3.5 mmol), N,O-dimethylhydroxylamine hydrochloride (0.52 g, 5.3 mmol), TEA (1.5 ml, 11 mmol) and O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium tetrafluoroborate (1.2 g, 3.9 mmol) in DMF (15 ml) was stirred at room temperature overnight. The mixture was diluted with AcOEt. The precipitate was filtered off and the filtrate was concentrated under reduced pressure. The residue was chromatographed on basic silica gel (0/100-20/80 MeOH/AeOEt) to give the title compound (0.81 g, 79% yield) as white crystals: 1H NMR (300 MHz, CDCl3): δ ppm 3.41 (3H, s), 3.71 (3H, s), 3.98 (3H, s), 7.48 (1H, dd, J=8.3, 4.5 Hz), 7.97 (1H, s), 8.00-8.05 (1H, m), 8.67 (1H, dd, J=4.5, 1.3 Hz), 8.91 (1H, d, J=2.6 Hz).

Workup

  1. filtrationThe precipitate was filtered off
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe residue was chromatographed on basic silica gel (0/100-20/80 MeOH/AeOEt)

Sources & evidence

ORD record
ord-afb2f65a42494ab0a4c5e3d1b181059c
Source dataset
uspto-grants-2014_07
Patent number
US08778944B2

Reaction notes

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