Sodium hydride → HCID 18326226, compound

HRID 1250491Notes

Reaction equation

[F:1][C:2]([F:12])([F:11])[S:3][C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1.[H-].[Na+].[CH:15]([NH:18][C:19]([C:21]1[CH:26]=[C:25]([O:27][CH3:28])[CH:24]=[C:23](Br)[N:22]=1)=[O:20])([CH3:17])[CH3:16]>CN(C=O)C.C(OCC)(=O)C.[Cu](Cl)Cl>[CH:15]([NH:18][C:19]([C:21]1[CH:26]=[C:25]([O:27][CH3:28])[CH:24]=[C:23]([O:10][C:6]2[CH:7]=[CH:8][CH:9]=[C:4]([S:3][C:2]([F:11])([F:1])[F:12])[CH:5]=2)[N:22]=1)=[O:20])([CH3:17])[CH3:16]

Participants

Conditions

Temperature: 110 °C

Procedure

1.25 g (0.0029×2.2 mol) of 3-(trifluoromethylthio) phenol was dissolved in about 10 ml of DMF. The obtained solution was further mixed with 0.23 g (ca. 60% in mineral oil; 0.0029×2.0 mol) of NaH and then with 0.80 g (0.0029 mol) of N-(i-propyl)-6-bromo-4-methoxy-2-pyridine carboxamide. After adding 0.15 g (0.0029×0.5 mol) of copper chloride (I), the obtained solution was stirred at about 110° C. for about 6 hours, and then allowed to stand for cooling to room temperature. After the reaction solution was distributed in ethyl acetate-saturated sodium bicarbonate water, the organic phase of the solution was washed with saturated brine and dried with anhydrous sodium sulfate, followed by concentration thereof. Thereafter, the concentrated solution was purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.

Workup

temperaturefor cooling to room temperature
washthe organic phase of the solution was washed with saturated brine
dry with materialdried with anhydrous sodium sulfate
concentrationfollowed by concentration
customThereafter, the concentrated solution was purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane)

Sources & evidence

ORD record: ord-91e7c665e8a24f4199a8e48d3182d05e
Source dataset: uspto-grants-2002_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06339045B1

Reaction notes

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