Ethyl Acetate → HCID 91176746, compound
Reaction equation
[OH:1][CH2:2][CH2:3][S:4]([CH2:7][CH2:8][O:9][C:10]([O:12][C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=1)=[O:11])(=[O:6])=[O:5].[NH2:22][CH2:23][CH2:24][CH2:25][NH:26][C:27]([C:40]1[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[CH:42][CH:41]=1)([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.[C:48](OCC)(=[O:50])C>>[N+:19]([C:16]1[CH:17]=[CH:18][C:13]([O:12][C:10]([O:9][CH2:8][CH2:7][S:4]([CH2:3][CH2:2][O:1][C:48](=[O:50])[NH:22][CH2:23][CH2:24][CH2:25][NH:26][C:27]([C:40]2[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[CH:42][CH:41]=2)([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)(=[O:6])=[O:5])=[O:11])=[CH:14][CH:15]=1)([O-:21])=[O:20]Participants
Procedure
A solution of 18 (0.68 g, 2.13 mmol) and (3-aminopropyl)[(4-methoxyphenyl)diphenylmethyl]amine (0.89 g, 2.56 mmol) was stirred at 40° C. for 30 min. p-nitrophenyl chlorofornate (0.62 g, 3.08 mmol) was added and stirring was continued for an additional 2 h. The solution was diluted with ethyl acetate (350 ml), washed with water (300 ml) and then dried over sodium sulfate and evaporated. The residue was purified by silica gel chromatography eluting with a gradient of 40-100% ethyl acetate in hexane. The pure product fractions were evaporated affording a foam: 351 mg of 20 (35%) yield; 1H NMR (DMSO-d6) δ 8.32 (2H, d, J=9.2 Hz, aromatic), 7.56 (1H, d, J=9.2 Hz, aromatic), 7.37 (4H, d, J=7.4 Hz, aromatic), 7.29-7.15 (8H, m, aromatic), 6.83 (2H, d, J=8.9 Hz, aromatic), 4.61 (2H, t, J=5.5 Hz, CH2), 4.29 (2H, t, J=6.0 Hz, CH2), 3.71 (3H, s, methoxy), 3.67 (2H, t, J=5.7 Hz, CH2), 3.51 (2H, t, J=5.8 Hz, CH2), 3.07 (2H, m, CH2), 1.93 (2H, m, CH2), 1.59 (2H, m, CH2).
Workup
- additionwas added
- washwashed with water (300 ml)
- dry with materialdried over sodium sulfate
- customevaporated
- customThe residue was purified by silica gel chromatography
- washeluting with a gradient of 40-100% ethyl acetate in hexane
- customThe pure product fractions were evaporated
- customaffording a foam
Sources & evidence
- ORD record
- ord-79aa2e5990bf4d47910fb9b4ba41d829
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472153B1
Reaction notes
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