Hydrochloric Acid → HCID 66825853, compound

HRID 2177959Notes

Reaction equation

HRID 2177959 reaction equation
[C:1]1([CH2:7][C:8]([C:10]2[CH:14]=[CH:13][N:12]([S:15]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)(=[O:17])=[O:16])[CH:11]=2)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:24]([O:26][C:27]1[CH:28]=[C:29]([CH:32]=[C:33]([N+:36]([O-:38])=[O:37])[C:34]=1[OH:35])[CH:30]=O)[CH3:25].[NH2:39][C:40]([NH2:42])=[O:41].Cl>C(O)C>[CH2:24]([O:26][C:27]1[CH:28]=[C:29]([CH:30]2[C:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[C:8]([C:10]3[CH:14]=[CH:13][N:12]([S:15]([C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)(=[O:17])=[O:16])[CH:11]=3)[NH:42][C:40](=[O:41])[NH:39]2)[CH:32]=[C:33]([N+:36]([O-:38])=[O:37])[C:34]=1[OH:35])[CH3:25]

Participants

6

Procedure

To a solution of 2-phenyl-1-(1-(phenylsulfonyl)-1H-pyrrol-3-yl)ethanone (Intermediate 52) (200 mg, 0.6 mmol), 3-ethoxy-4-hydroxy-5-nitrobenzaldehyde (130 mg, 0.6 mmol), and urea (108 mg, 1.8 mmol) in 10 mL of ethanol was added 0.2 mL of concentrated HCl solution. The mixture refluxed overnight, concentrated in vacuo, and purified by TLC (PE:EtOAc=1:2) to afford the Compound 107 (95 mg, yield 27.6%). 1H NMR (DMSO-d6 400 MHz): δ10.25 (s, 1H), 8.53 (s, 1H), 7.86 (d, J=7.6 Hz, 2H), 7.77 (t, J=7.6 Hz, 1H), 7.65 (t, J=8.0 Hz, 2H), 7.49 (s, 1H), 7.36 (s, 1H), 7.31 (d, J=2.0 Hz, 1H), 7.17-7.14 (m, 3H), 7.12 (t, J=2.8 Hz, 1H), 7.00 (d, J=2.0 Hz, 1H), 6.91-6.89 (m, 2H), 5.70 (m, 1H), 5.10 (d, J=2.4 Hz, 1H), 4.05-3.90 (m, 2H), 1.29 (t, J=7.2 Hz, 3H); MS (ESI): m/z 561.3 [M+1]+.

Workup

  1. temperatureThe mixture refluxed overnight
  2. concentrationconcentrated in vacuo
  3. custompurified by TLC (PE:EtOAc=1:2)

Sources & evidence

ORD record
ord-a59307f6a66042b18692f93be74f3ff2
Source dataset
uspto-grants-2015_06
Patent number
US09067893B2

Reaction notes

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