Ethyl isocyanate → HCID 11656805, compound
Reaction equation
[NH2:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([N:12]([CH2:24][CH2:25][CH2:26][N:27]3[CH2:32][CH2:31][N:30]([CH3:33])[CH2:29][CH2:28]3)[C:13]([NH:15][C:16]3[CH:21]=[CH:20][C:19]([F:22])=[C:18]([Cl:23])[CH:17]=3)=[O:14])[CH2:9]2)=[CH:4][CH:3]=1.[CH2:34]([N:36]=[C:37]=[O:38])[CH3:35]>C(Cl)Cl>[Cl:23][C:18]1[CH:17]=[C:16]([NH:15][C:13](=[O:14])[N:12]([CH:8]2[CH2:9][C:10]3[CH:11]=[C:2]([NH:1][C:37]([NH:36][CH2:34][CH3:35])=[O:38])[CH:3]=[CH:4][C:5]=3[CH2:6][CH2:7]2)[CH2:24][CH2:25][CH2:26][N:27]2[CH2:28][CH2:29][N:30]([CH3:33])[CH2:31][CH2:32]2)[CH:21]=[CH:20][C:19]=1[F:22]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1-(7-amino-1,2,3,4-tetrahydro-naphthalen-2-yl)-3-(3-chloro-4-fluoro-phenyl)-1-[3-(4-methyl-piperazin-1-yl)-propyl]-urea (from Preparative Example 27, 0.018 g, 0.038 mmol) in CH2Cl2 (0.2 mL) at 0° C. was added ethylisocyanate (0.0030 mL, 0.038 mmol). The mixture was stirred from 0° C. to room temperature for 16 hours, then concentrated in vacuo, and the residue was purified by preparative HPLC to give 0.019 g (92%) of 1-(7-{3-(3-chloro-4-fluoro-phenyl)-1-[3-(4-methyl-piperazin-1-yl)-propyl]-ureido}-5,6,7,8-tetrahydro-naphthalen-2-yl)-3-ethyl-urea as a light yellow gum. 1H NMR (300 MHz, CD3OD): δ 7.60 (dd, 1H, J=6.6, 2.4 Hz), 7.30 (ddd, 1H, J=9.0, 4.2, 2.7 Hz), 7.18 (s, 1H), 7.15 (t, 1H, J=9.0 Hz), 7.06-6.97 (m, 2H), 4.30 (m, 1H), 3.60-3.40 (m, 10H), 3.20 (m, 4H), 3.05-2.85 (m, 7H), 2.07 (m, 4H), 1.15 (t, 3H, J=7.5 Hz). MS-ESI: 545.0 (M+H+).
Workup
- concentrationconcentrated in vacuo
- customthe residue was purified by preparative HPLC
Sources & evidence
- ORD record
- ord-8ed8784518514ebb8ec00d3da1474500
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07550467B2
Reaction notes
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