4-(Dimethylamino)phenyl isocyanate → HCID 46865173, compound
Reaction equation
[CH2:1]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([OH:17])=[CH:14][CH:15]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:18][N:19]([CH3:29])[C:20]1[CH:25]=[CH:24][C:23]([N:26]=[C:27]=[O:28])=[CH:22][CH:21]=1>>[CH3:18][N:19]([CH3:29])[C:20]1[CH:25]=[CH:24][C:23]([NH:26][C:27](=[O:28])[O:17][C:13]2[CH:12]=[C:11]3[C:16](=[CH:15][CH:14]=2)[N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:9][CH2:10]3)=[CH:22][CH:21]=1Participants
3
Procedure
The title compound was synthesized from 1-benzylindolin-5-ol (45.0 mg, 0.200 mmol) using the same procedure employed for Example 2 (2), but with 4-dimethylaminophenylisocyanate instead of 4-isopropylphenylisocyanate. The product was obtained as a slightly brown solid (34.8 mg, 45%) having the following characteristics.
Sources & evidence
- ORD record
- ord-41f13c9504384cb6877334ba0d6b629d
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686024B2
Reaction notes
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