Hydroxylamine → HCID 86620213, compound
Reaction equation
[Si:1]([O:8][CH2:9][C:10]1[S:14][C:13]([C:15]#[N:16])=[CH:12][CH:11]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[NH2:17][OH:18]>>[Si:1]([O:8][CH2:9][C:10]1[S:14][C:13]([C:15](=[N:17][OH:18])[NH2:16])=[CH:12][CH:11]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]Participants
3
Procedure
The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 1 (1d) using 5-({[t-butyl(dimethyl)silyl]oxy}methyl)thiophene-2-carbonitrile (1.3 g, 5.0 mmol) that was obtained in Example 4 (4a) and a 40% aqueous solution of hydroxylamine (0.7 ml). Subsequently, the crude product of the title compound thus obtained was purified by recrystallization from a mixed solvent of ethyl acetate and hexane to afford the title compound (1.2 g) in a yield of 81% as a white crystalline solid.
Workup
- customthe similar reaction to
Sources & evidence
- ORD record
- ord-635c0b18d1be449293d3418eb2c65432
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687491B2
Reaction notes
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