Bosutinib → HCID 86610056, compound

HRID 499132Notes

Reaction equation

HRID 499132 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([O:9][CH3:10])=[CH:4][C:3]=1[NH:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([O:24][CH2:25][CH2:26][CH2:27][N:28]3[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]3)=[C:19]([O:22][CH3:23])[CH:20]=2)[N:15]=[CH:14][C:13]=1[C:35]#[N:36]>C(O)(C)C.O>[CH:5]([O-:9])([CH3:6])[CH3:4].[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([O:9][CH3:10])=[CH:4][C:3]=1[NH:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([O:24][CH2:25][CH2:26][CH2:27][N:28]3[CH2:33][CH2:32][N:31]([CH3:34])[CH2:30][CH2:29]3)=[C:19]([O:22][CH3:23])[CH:20]=2)[N:15]=[CH:14][C:13]=1[C:35]#[N:36]

Participants

3

Procedure

4-[(2,4-Dichloro-5-methoxyphenyl)amino]-6-methoxy-7-[3-(4-methyl-1-piperazinyl)propoxy]-3-quinolinecarbonitrile (5 g) and 40 mL of a mixture of 2/1 isopropyl alcohol/water (v/v) were added to a 125 flask, and heated to reflux. The mixture was cooled over night to room temperature and filtered. The cake was washed with 15 mL of a 2/1 mixture of isopropyl alcohol/water (v/v) and vacuum dried at 45° C. to give 4.51 g of 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-methoxy-7-[3-(4-methyl-1-piperazinyl)propoxy]-3-quinolinecarbonitrile monoisopropyl alcoholate as determined by GLC and NMR and determined to be Form III by XRD scans.

Workup

  1. temperatureheated to reflux
  2. filtrationfiltered
  3. washThe cake was washed with 15 mL of a 2/1 mixture of isopropyl alcohol/water (v/v) and vacuum
  4. customdried at 45° C.

Sources & evidence

ORD record
ord-e321b645f8c8482dbf24be9b981e8f33
Source dataset
uspto-grants-2010_08
Patent number
US07767678B2

Reaction notes

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