5-Amino-2-methylphenol → HCID 10198953, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:15]3=[CH:16][C:17](C)=[CH:18][N:14]3[N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[CH3:8].O[C:21]1C=C(C=CC=1C)N>>[OH:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:15]3=[CH:16][CH:17]=[C:18]([CH3:21])[N:14]3[N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[CH3:8]Participants
3
Procedure
Example 11 was prepared as a white solid in 30% overall yield from Compound E using the 2 step sequence of Compound A of Example 1 and Compound B of Example 1, using 3-hydroxy-4-methylaniline. The product was purified by flash chromatography on silica with 25% ethyl acetate/hexanes. (M+H)+255.
Workup
- customExample 11 was prepared as a white solid in 30%
- customThe product was purified by flash chromatography on silica with 25% ethyl acetate/hexanes
Sources & evidence
- ORD record
- ord-65507a52607847688fb11989abe36954
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06982265B1
Reaction notes
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