4-Hydroxybenzaldehyde → HCID 69516270, compound
Reaction equation
[O:1]=[C:2]1[NH:6][CH2:5][C:4](=[O:7])[N:3]1[C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11]([C:18]#[N:19])=[CH:10][CH:9]=1.[OH:20][C:21]1[CH:28]=[CH:27][C:24]([CH:25]=O)=[CH:23][CH:22]=1>>[OH:20][C:21]1[CH:28]=[CH:27][C:24]([CH:25]=[C:5]2[C:4](=[O:7])[N:3]([C:8]3[C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[C:11]([C:18]#[N:19])=[CH:10][CH:9]=3)[C:2](=[O:1])[NH:6]2)=[CH:23][CH:22]=1Participants
3
Procedure
The title compound was obtained as an off-white solid (37.3 mg, 17.6%), mp>275° C. from compound 1C and 4-hydroxybenzaldehyde in the same manner as that used in the preparation of Example 1 by acidifying the aqueous washings and recrystallization of the crude product from MeOH. LC/MS m/z 356 [M+H]+.
Sources & evidence
- ORD record
- ord-6df4a666734349d39a2d6b2a41ee5c98
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07256208B2
Reaction notes
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