Diethylamine → HCID 58931308, compound

HRID 853585Notes

Reaction equation

HRID 853585 reaction equation
CC1C=CC(S(O[CH2:12][C@H:13]2[CH2:15][O:14]2)(=O)=O)=CC=1.C(=O)([O-])[O-].[K+].[K+].[CH2:22]([NH:24][C:25]([C:27]1[CH:28]=[C:29]2[C:34](=[CH:35][C:36]=1[OH:37])[N:33]=[CH:32][CH:31]=[C:30]2[O:38][C:39]1[CH:44]=[CH:43][C:42]([NH:45][C:46]([NH:48][CH3:49])=[O:47])=[C:41]([Cl:50])[CH:40]=1)=[O:26])[CH3:23].[CH2:51]([NH:53][CH2:54][CH3:55])[CH3:52]>O.C(OCC)(=O)C.O1CCCC1.CN(C)C=O>[CH2:22]([NH:24][C:25]([C:27]1[CH:28]=[C:29]2[C:34](=[CH:35][C:36]=1[O:37][CH2:15][C@H:13]([OH:14])[CH2:12][N:53]([CH2:54][CH3:55])[CH2:51][CH3:52])[N:33]=[CH:32][CH:31]=[C:30]2[O:38][C:39]1[CH:44]=[CH:43][C:42]([NH:45][C:46]([NH:48][CH3:49])=[O:47])=[C:41]([Cl:50])[CH:40]=1)=[O:26])[CH3:23]

Participants

8

Reactant 4

HCID 8021DiethylamineHCID 11430Potassium CarbonateHCID 154187Glycidyl tosylate, (R)-HCID 135829396HCID 135829396, compound

Product 1

HCID 58931308HCID 58931308, compoundYield 49.3%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 6228DimethylformamideSolventHCID 21939870Tetrahydrofuran ethyl acetateSolvent

Conditions

Temperature
60 °C

Procedure

After adding (2R)oxiran-2-ylmethyl 4-methyl-1-benzenesulfonate (66 mg, 0.290 mmol), potassium carbonate (32 mg, 0.231 mmol) and dimethylformamide (2 ml) to N6-ethyl-4-(3-chloro-4-(((methylamino)carbonyl)amino)phenoxy)-7-hydroxy-6-quinolinecarboxamide (80.0 mg, 0.193 mmol), the mixture was stirred at 60° C. for 7 hours. Diethylamine (1 ml) was then added, and the mixture was stirred at 60° C. overnight. The reaction solution was distributed between ethyl acetate-tetrahydrofuran (1:1) and water, and the organic layer was washed with water and saturated brine and then dried over anhydrous sodium sulfate. The solvent was distilled off, the residue was subjected to silica gel column chromatography (eluent—ethyl acetate:methanol=95:5), the fraction containing the target substance was concentrated, and crystals were precipitated from ethyl acetate-hexane (1:1), filtered out and blow-dried to obtain the title compound (51.7 mg, 0.095 mmol, 49.3%) as white crystals.

Workup

  1. stirringthe mixture was stirred at 60° C. overnight
  2. washthe organic layer was washed with water and saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. distillationThe solvent was distilled off
  5. additionthe fraction containing the target substance
  6. concentrationwas concentrated
  7. customcrystals were precipitated from ethyl acetate-hexane (1:1)
  8. filtrationfiltered out and
  9. customblow-dried

Sources & evidence

ORD record
ord-af26190b6fee4bc9bcff71e3b26cf0c0
Source dataset
uspto-grants-2007_08
Patent number
US07253286B2

Reaction notes

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