4-Ethylphenyl isocyanate → HCID 58659386, compound
Reaction equation
[NH2:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][C:7]2[CH:12]=[CH:11][N:10]=[C:9]([O:13][CH3:14])[CH:8]=2)=[CH:4][CH:3]=1.[CH2:17]([C:19]1[CH:24]=[CH:23][C:22]([N:25]=[C:26]=[O:27])=[CH:21][CH:20]=1)[CH3:18]>>[CH3:14][O:13][C:9]1[CH:8]=[C:7]([O:6][C:5]2[CH:15]=[CH:16][C:2]([NH:1][C:26]([NH:25][C:22]3[CH:23]=[CH:24][C:19]([CH2:17][CH3:18])=[CH:20][CH:21]=3)=[O:27])=[CH:3][CH:4]=2)[CH:12]=[CH:11][N:10]=1Participants
3
Procedure
The title compound is prepared from 4-(4-amino-phenoxy)-2-methoxy-pyridine (Stage 92.1; 91 mg, 0.42 mmol) and 4-ethyl-phenyl-isocyanate (124 μl, 0.84 mmol) analogously to Example 89: m.p.: 196° C.; Anal.: CHN.
Sources & evidence
- ORD record
- ord-cb69accd58e94a098a0c6af38868e8be
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07652022B2
Reaction notes
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