Trifluoroacetic acid → HCID 58025839, Verbindung

HRID 1046945Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1046945
C(O[C:6]([NH:8][NH:9][C:10]([C:12]1[CH:13]=[N:14][C:15]([F:18])=[CH:16][CH:17]=1)=[S:11])=[O:7])(C)(C)C.C(OC(NNC(=O)C1C=CC(F)=CC=1)=O)(C)(C)C.C(O)(C(F)(F)F)=O.C1(SC)C=CC=CC=1.CCN(C(C)C)C(C)C.[F:61][CH:62]([F:72])[O:63][C:64]1[CH:71]=[CH:70][CH:69]=[CH:68][C:65]=1[CH:66]=O.[F:73][C:74]1[CH:82]=[C:81]([F:83])[CH:80]=[C:79]([F:84])[C:75]=1C(Cl)=O>C(Cl)Cl>[F:61][CH:62]([F:72])[O:63][C:64]1[CH:71]=[CH:70][CH:69]=[CH:68][C:65]=1[CH:66]1[N:8]([C:6]([C:75]2[C:74]([F:73])=[CH:82][C:81]([F:83])=[CH:80][C:79]=2[F:84])=[O:7])[N:9]=[C:10]([C:12]2[CH:13]=[N:14][C:15]([F:18])=[CH:16][CH:17]=2)[S:11]1

Komponenten

9

Edukt 7

HCID 6422Trifluoroacetic acidHCID 7520ThioanisoleHCID 81531DiisopropylethylamineHCID 1448952,4,6-Trifluorobenzoyl chlorideHCID 27369842-(Difluoromethoxy)benzaldehydeHCID 67279032tert-Butyl 2-(4-fluorobenzoyl)hydrazine-1-carboxylateHCID 86637599HCID 86637599, Verbindung

Produkt 1

HCID 58025839HCID 58025839, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

N′-(6-fluoro-pyridine-3-carbothioyl)-hydrazinecarboxylic acid tert-butyl ester (0.044 mmol) prepared as described in example 3 for N′-(4-fluoro-benzoyl)-hydrazinecarboxylic acid tert-butyl ester, is treated with TFA (0.44 mmol) and thioanisole (0.44 mmol) in dry CH2Cl2 (1 mL) at room temperature for 30 minutes. The solvent is removed and the residue is dissolved in dry CH2Cl2 (1 mL). DIEA (0.22 mmol) is added to the solution and the mixture is treated with 2-difluoromethoxy-benzaldehyde (0.067 mmol) in the presence of 4 Å molecular sieves. 2,4,6-Trifluorobenzoyl chloride (0.089 mmol) is added after 5 minutes. The mixture is kept at room temperature for 16 hours and purified by preparative silica gel TLC (30% EtOAc/hexane) to yield [2-(2-difluoromethoxy-phenyl)-5-(6-fluoro-pyridin-3-yl)-[1,3,4]thiadiazol-3-yl]-(2,4,6-trifluoro-phenyl)-methanone: 1H NMR (400 MHz, CDCl3) 8.39 (s, 1H), 7.93-7.97 (m, 1H), 7.54 (s, 1H), 7.37-7.41 (m, 2H), 7.24-7.27 (m, 1H), 7.19 (d, J=8.1 Hz, 1H), 6.97 (dd, J1=8.6 Hz, J2=2.7 Hz, 1H), 6.78 (t, J=8.3 Hz, 2H), 6.67 (dd, J1=75.0 Hz, J2=71.7 Hz, 1H); LC/MS (ES+): (M+1) 484.1.

Aufarbeitung

  1. customThe solvent is removed
  2. dissolutionthe residue is dissolved in dry CH2Cl2 (1 mL)
  3. custompurified by preparative silica gel TLC (30% EtOAc/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-bbdbb2a885d84255b50a3f93f043ce2f
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08569345B2

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