Water → HCID 68800023, compound

HRID 1884396Notes

Reaction equation

HRID 1884396 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:15](=[O:16])[C:14]2[C:9](=[CH:10][C:11]([Br:19])=[C:12]([CH2:17]Br)[CH:13]=2)[N:8]([CH2:20][C:21]2[C:26]([F:27])=[CH:25][CH:24]=[CH:23][C:22]=2[F:28])[CH:7]=1)=[O:5])[CH3:2].[CH3:29][NH:30][CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1.C(OCC)(=O)C.O>CCN(C(C)C)C(C)C.CN(C=O)C>[CH2:1]([O:3][C:4]([C:6]1[C:15](=[O:16])[C:14]2[C:9](=[CH:10][C:11]([Br:19])=[C:12]([CH2:17][N:30]([CH2:31][C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[CH3:29])[CH:13]=2)[N:8]([CH2:20][C:21]2[C:22]([F:28])=[CH:23][CH:24]=[CH:25][C:26]=2[F:27])[CH:7]=1)=[O:5])[CH3:2]

Participants

7

Procedure

A mixture of 7-bromo-6-bromomethyl-1-(2,6-difluorobenzyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid ethyl ester (110 mg, 0.21 mmol), methylbenzylamine (31 mg, 0.26 mmol) in DIPEA (0.045 mL) and DMF (15 mL) was stirred at room temperature for 16 h. Ethyl acetate and water were added. The organic phase was separated and washed with water, dried with MgSO4. The solvent was evaporated and the residue dried under vacuum to yield the product as a white solid.

Workup

  1. customThe organic phase was separated
  2. washwashed with water
  3. dry with materialdried with MgSO4
  4. customThe solvent was evaporated
  5. customthe residue dried under vacuum

Sources & evidence

ORD record
ord-f39cada8593e4c41ba8ce914ccf15319
Source dataset
uspto-grants-2004_07
Patent number
US06765011B2

Reaction notes

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