Ethyl Propionate → HCID 67259334, compound

HRID 908033Notes

Reaction equation

HRID 908033 reaction equation
O=C1C2[C:5](=[C:6](/[N:11]=[CH:12]/[C:13]3[CH:18]=[CH:17][C:16]([CH:19]4[CH2:23][CH2:22][CH2:21][N:20]4[C:24]([O:26][CH2:27][C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=4)=[O:25])=[CH:15][CH:14]=3)C=CC=2)[CH2:4]O1.[F:34][C:35]1[CH:42]=[CH:41][C:38]([CH:39]=O)=[CH:37][CH:36]=1.[CH3:43][CH2:44][O-:45].[Na+].[C:47]([O:51][CH2:52][CH3:53])(=[O:50])[CH2:48][CH3:49]>CCO>[CH2:27]([O:26][C:24]([N:20]1[CH2:21][CH2:22][CH2:23][CH:19]1[C:16]1[CH:17]=[CH:18][C:13]([CH:12]2[CH:39]([C:38]3[CH:41]=[CH:42][C:35]([F:34])=[CH:36][CH:37]=3)[C:44](=[O:45])[C:43]3[C:48]([C:47]([O:51][CH2:52][CH3:53])=[O:50])=[CH:49][CH:4]=[CH:5][C:6]=3[NH:11]2)=[CH:14][CH:15]=1)=[O:25])[C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1

Participants

6

Procedure

A solution of (E)-benzyl 2-(4-((1-oxo-1,3-dihydroisobenzofuran-4-ylimino)methyl)phenyl)pyrrolidine-1-carboxylate (0.5 g, 1.14 mmol) and 4-fluoro benzaldehyde (0.284 g, 2.28 mmol) in dry ethyl propionate (5 mL) was added EtONa (0.155 g, 2.28 mmol) in EtOH (6 mL), and the mixture was stirred at room temperature until the starting material was disappeared as monitored by TLC. Then the reaction mixture was quenched with 0.5 mL of water, the resulting mixture was concentrated in vacuo, and the residue was purified by column chromatography to give the title compound (130 mg, yield 20%) as a yellow solid. LC-MS (ESI) m/z: 592(M+1)+.

Workup

  1. customThen the reaction mixture was quenched with 0.5 mL of water
  2. concentrationthe resulting mixture was concentrated in vacuo
  3. customthe residue was purified by column chromatography

Sources & evidence

ORD record
ord-7ad2cfb4dd6d443694bbfcb33a49f659
Source dataset
uspto-grants-2011_09
Patent number
US08012976B2

Reaction notes

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