Acetic Acid → HCID 22238162, compound

HRID 1743132Notes

Reaction equation

HRID 1743132 reaction equation
[Cl:1][C:2]1[CH:23]=[CH:22][C:5]([C:6]([NH:8][C:9]2[CH:14]=[C:13]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:12]=[C:11]([F:21])[CH:10]=2)=[O:7])=[CH:4][C:3]=1[NH:24][C:25](=[O:42])[C:26]1[CH:31]=[C:30]([N:32]2[CH2:37][CH2:36][N:35]([CH3:38])[CH2:34][CH2:33]2)[CH:29]=[CH:28][C:27]=1[N+:39]([O-])=O.C(O)(=O)C.C(=O)([O-])[O-].[Na+].[Na+]>[Fe].O.C(O)C>[NH2:39][C:27]1[CH:28]=[CH:29][C:30]([N:32]2[CH2:37][CH2:36][N:35]([CH3:38])[CH2:34][CH2:33]2)=[CH:31][C:26]=1[C:25]([NH:24][C:3]1[CH:4]=[C:5]([CH:22]=[CH:23][C:2]=1[Cl:1])[C:6]([NH:8][C:9]1[CH:14]=[C:13]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[CH:12]=[C:11]([F:21])[CH:10]=1)=[O:7])=[O:42]

Participants

7

Procedure

Iron powder (0.726 g) was added to a stirred suspension of 4-chloro-N-(3-fluoro-5-morpholinophenyl)-3-[5-(4-methylpiperazin-1-yl)-2-nitrobenzamido]benzamide (0.76 g), water (2 ml), acetic acid (0.5 ml) and ethanol (15 ml) and the resultant mixture was stirred and heated to reflux for 1 hour. The mixture was cooled to ambient temperature. Water (80 ml) was added and the mixture was basified by the addition of sodium carbonate. The resultant mixture was filtered through diatomaceous earth and the separated solids were washed in turn with methylene chloride and methanol. The combined filtrates were evaporated and the residue was triturated under ethyl acetate. The mixture was filtered and the filtrate was evaporated to give 3-[2-amino-5-(4-methylpiperazin-1-yl)benzamido]-4-chloro-N-(3-fluoro-5-morpholinophenyl)benzamide (0.385 g); Mass Spectrum: M+H+ 567.

Workup

  1. temperatureheated
  2. temperatureto reflux for 1 hour
  3. filtrationThe resultant mixture was filtered through diatomaceous earth
  4. washthe separated solids were washed in turn with methylene chloride and methanol
  5. customThe combined filtrates were evaporated
  6. customthe residue was triturated under ethyl acetate
  7. filtrationThe mixture was filtered
  8. customthe filtrate was evaporated

Sources & evidence

ORD record
ord-f1e1628e44a1475f8920e735ff11a433
Source dataset
uspto-grants-2006_03
Patent number
US07008945B1

Reaction notes

Loading…