O-Methylhydroxylamine hydrochloride → HCID 87417166, compound
Reaction equation
[CH:1]([C:3]1[CH:23]=[CH:22][C:6]2[N:7]([C:10]3[CH:15]=[CH:14][CH:13]=[C:12]([C:16]4[N:21]=[CH:20][CH:19]=[CH:18][N:17]=4)[CH:11]=3)[CH:8]=[N:9][C:5]=2[CH:4]=1)=O.[NH2:24][O:25][CH3:26].Cl>>[CH3:26][O:25][N:24]=[CH:1][C:3]1[CH:23]=[CH:22][C:6]2[N:7]([C:10]3[CH:15]=[CH:14][CH:13]=[C:12]([C:16]4[N:17]=[CH:18][CH:19]=[CH:20][N:21]=4)[CH:11]=3)[CH:8]=[N:9][C:5]=2[CH:4]=1Participants
3
Procedure
was synthesized as described in Example 22 but using (68) (210 mg, 0.70 mmol) instead of (55) and NH2OMe.HCl (300 mg, 3.6 mmol) instead of NH2OH.HCl. The reaction gave (69) (192 mg, 83%). Mp. 158-159° C.
Workup
- customwas synthesized
Sources & evidence
- ORD record
- ord-6bf1885cdd3745fc8ef3cad3a0a1c077
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05922725
Reaction notes
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