4-Hydrazinobenzoic acid → Deferasirox

HRID 1092193Notes

Reaction equation

HRID 1092193 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[O:9][C:10]2[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=2[C:12](=O)[N:13]=1.[NH:19]([C:21]1[CH:29]=[CH:28][C:24]([C:25]([OH:27])=[O:26])=[CH:23][CH:22]=1)[NH2:20]>CN(C)C=O.C(O)(=O)CC>[CH:16]1[CH:17]=[CH:18][C:10]([OH:9])=[C:11]([C:12]2[N:13]=[C:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[OH:1])[N:19]([C:21]3[CH:29]=[CH:28][C:24]([C:25]([OH:27])=[O:26])=[CH:23][CH:22]=3)[N:20]=2)[CH:15]=1

Participants

5

Reactant 2

HCID 120894-Hydrazinobenzoic acidHCID 1356857232-(2-Hydroxyphenyl)-4H-1,3-benzoxazin-4-one

Product 1

HCID 214348DeferasiroxYield 80.7%

Reagents, catalysts & solvents 2

HCID 1032Propionic AcidSolventHCID 6228DimethylformamideSolvent

Conditions

Temperature
150 °C

Procedure

A suspension of 0.7 g (2.92 mmol) of 2-(2-hydroxyphenyl)benz[e][1,3]oxazin-4-one and 0.52 g (3.44 mmol) of 4-hydrazinobenzoic acid in 5 ml of N,N-dimethylformamide and 5 ml of propionic acid is heated up to 150° C. The mixture is maintained at this temperature and stirred for 1.5 hours. After completion of the reaction, the mixture is cooled and poured onto crushed ice. The resulting crystals are aspirated and washed with water. After drying, 0.88 g of raw deferasirox is obtained, i.e. 81% of the theory, with an HPLC purity of 93% and a melting temperature of 255 to 262° C.

Workup

  1. temperatureThe mixture is maintained at this temperature
  2. customAfter completion of the reaction
  3. temperaturethe mixture is cooled
  4. additionpoured
  5. customonto crushed ice
  6. washwashed with water
  7. customAfter drying

Sources & evidence

ORD record
ord-bf3255472b0c44e5aa21487e7745a11c
Source dataset
uspto-grants-2012_03
Patent number
US08129421B2

Reaction notes

Loading…