Hydrochloric Acid → HCID 178489125, compound

HRID 895358Notes

Reaction equation

HRID 895358 reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[C:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:10][C:9]([NH2:18])=[CH:8][CH:7]=1.[N:19]([O-])=O.[Na+].Cl.[CH3:24][O:25][C:26]1[CH:27]=[C:28]([C:34]2[CH2:35][C:36](=[O:39])[NH:37][N:38]=2)[CH:29]=[CH:30][C:31]=1[O:32][CH3:33].C([O-])(=O)C.[Na+]>O.C(O)C>[Br:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[C:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:10][C:9]([NH:18][N:19]=[C:35]2[C:34]([C:28]3[CH:29]=[CH:30][C:31]([O:32][CH3:33])=[C:26]([O:25][CH3:24])[CH:27]=3)=[N:38][NH:37][C:36]2=[O:39])=[CH:8][CH:7]=1

Participants

7

Procedure

6-(3-Bromo-propoxy)-biphenyl-3-ylamine (r, 250 mg, 0.82 mmol) was diazotized with sodium nitrite (67 mg, 0.98 mmol) in 1:1 water/ethanol and 0.5 mL concentrated HCl at 0° C. After approximately 1 hour, the diazonium solution was added dropwise to a suspension of 5-(3,4-dimethoxy-phenyl)-2,4-dihydro-pyrazol-3-one (200 mg, 0.9 mmol) and sodium acetate (1.1 g) in 10 mL 1:1 water/ethanol. The orange solid which precipitated was filtered and washed with water and dried. The crude product was purified by silica gel chromatography (eluent: 5% methanol/DCM) to afford 120 mg of 4-{[6-(3-bromo-propoxy)-biphenyl-3-yl]-hydrazono}-5-(3,4-dimethoxy-phenyl)-2,4-dihydro-pyrazol-3-one (s): HPLC (Rt) 5.02 min; m/e 536.1, MS (ES+): 538.9; 1H NMR (500 MHz, CDCl3): 13.9 (bs, 1H), 9.0 (bs, 1H), 7.7-6.9 (m, 11H), 4.1 (m, 2H), 3.9 (s, 3H), 3.7 (s, 3H), 3.5 (m, 2H), 3.3 (m, 2H), 2.2 (m, 2H) and 2.1 (m, 2H).

Workup

  1. customThe orange solid which precipitated
  2. filtrationwas filtered
  3. washwashed with water
  4. customdried
  5. customThe crude product was purified by silica gel chromatography (eluent: 5% methanol/DCM)

Sources & evidence

ORD record
ord-5c42b6987f7948fbaa95e8dc46a0e3d7
Source dataset
uspto-grants-2005_07
Patent number
US06916798B2

Reaction notes

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