Ethyl isothiocyanate → 7-(3,5-dimethyl-4-isoxazolyl)-N-ethyl-1-[1-methyl-2-(methyloxy)ethyl]-8-(methyloxy)-1H-imidazo[4,5-c]quinolin-2-amine
Reaction equation
[CH3:1][C:2]1[C:6]([C:7]2[CH:16]=[C:15]3[C:10]([C:11]([NH:18][CH:19]([CH3:23])[CH2:20][O:21][CH3:22])=[C:12]([NH2:17])[CH:13]=[N:14]3)=[CH:9][C:8]=2[O:24][CH3:25])=[C:5]([CH3:26])[O:4][N:3]=1.[N:27]([CH2:30][CH3:31])=[C:28]=S>>[CH3:1][C:2]1[C:6]([C:7]2[C:8]([O:24][CH3:25])=[CH:9][C:10]3[C:11]4[N:18]([CH:19]([CH3:23])[CH2:20][O:21][CH3:22])[C:28]([NH:27][CH2:30][CH3:31])=[N:17][C:12]=4[CH:13]=[N:14][C:15]=3[CH:16]=2)=[C:5]([CH3:26])[O:4][N:3]=1Participants
3
Procedure
From 7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-N4-(1-methoxypropan-2-yl)quinoline-3,4-diamine (for a preparation see Intermediate 17) (70 mg) and isothiocyanatoethane (50 mg) to give the title compound as beige solid (42 mg, 52%). LCMS (formate) Rt 0.78 min, MH+ 410
Sources & evidence
- ORD record
- ord-5305a2f38a9f48558823f25e0a2c503d
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846709B2
Reaction notes
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