Ethyl Acetate → HCID 91176746, compound

HRID 992911Notes

Reaction equation

HRID 992911 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

4

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

  1. additionwas added
  2. washwashed with water (300 ml)
  3. dry with materialdried over sodium sulfate
  4. customevaporated
  5. customThe residue was purified by silica gel chromatography
  6. washeluting with a gradient of 40-100% ethyl acetate in hexane
  7. customThe pure product fractions were evaporated
  8. customaffording a foam

Sources & evidence

ORD record
ord-79aa2e5990bf4d47910fb9b4ba41d829
Source dataset
uspto-grants-2002_10
Patent number
US06472153B1

Reaction notes

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