Ethyl isocyanate → HCID 57847093, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([C@H:7]2[C@H:16]3[CH2:17][CH2:18][N:19]([C:20]([C@H:22]4[CH2:27][CH2:26][CH2:25][CH2:24][C@H:23]4[NH:28][C:29](=[O:36])[C:30]4[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=4)=[O:21])[C@H:15]3[C:14]3[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=3[NH:8]2)[CH2:3][CH2:2]1.C(N(CC)CC)C.[CH2:44]([N:46]=[C:47]=[O:48])[CH3:45].O1CCCC1>O>[C:29]([NH:28][C@@H:23]1[CH2:24][CH2:25][CH2:26][CH2:27][C@@H:22]1[C:20]([N:19]1[C@@H:15]2[C@@H:16]([C@H:7]([CH:4]3[CH2:5][CH2:6][N:1]([C:47]([NH:46][CH2:44][CH3:45])=[O:48])[CH2:2][CH2:3]3)[NH:8][C:9]3[CH:10]=[CH:11][CH:12]=[CH:13][C:14]=32)[CH2:17][CH2:18]1)=[O:21])(=[O:36])[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of the compound (0.20 g, 0.41 mmol) synthesized in Example 69, triethylamine (0.17 g, 1.64 mmol), ethylisocyanate (0.058 g, 0.82 mmol) and tetrahydrofuran (20 ml) was stirred at room temperature for 60 hrs. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried (over anhydrous Na2SO4, and the solvent was evaporated under reduced pressure. The residue was recrystallized from hexane-ethyl acetate to give the title compound (0.20 g, 81%) as white crystals.
Workup
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with saturated brine
- dry with materialdried (over anhydrous Na2SO4
- customthe solvent was evaporated under reduced pressure
- customThe residue was recrystallized from hexane-ethyl acetate
Sources & evidence
- ORD record
- ord-23884bd45af944e2985c1961849a19ff
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07592453B2
Reaction notes
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