Pyridine → HCID 57920370, Verbindung

HRID 57179

Reaktionsgleichung

Reaktionsgleichung von HRID 57179
Cl.[CH3:2][C:3]1[C:4]2[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=2[S:6][C:7]=1[NH2:8].N1C=CC=CC=1.Cl[S:20]([C:23]1[CH:31]=[CH:30][C:26]([C:27]([OH:29])=[O:28])=[CH:25][CH:24]=1)(=[O:22])=[O:21]>C1COCC1.CCOC(C)=O>[CH3:2][C:3]1[C:4]2[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=2[S:6][C:7]=1[NH:8][S:20]([C:23]1[CH:24]=[CH:25][C:26]([C:27]([OH:29])=[O:28])=[CH:30][CH:31]=1)(=[O:22])=[O:21]

Komponenten

6

Edukt 3

HCID 1049PyridineHCID 823854-(Chlorosulfonyl)benzoic acidHCID 567239383-Methyl-1-benzothiophen-2-amine hydrochloride

Produkt 1

HCID 57920370HCID 57920370, VerbindungAusbeute 84,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittel2×HCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

A 12-L 4-neck flask equipped with an overhead mechanical stirrer, N2 inlet/outlet adapter, and thermocouple was charged with THF (3.26 L) and compound 757-A (326 g, 1.6 mol) followed by pyridine (265 mL, 3.3 mol). The reaction mixture was cooled to 5° C. using a ice bath, to which was added a solution of 4-(chlorosulfonyl)benzoic acid (396 g, 1.8 mol) dissolved in THF (2.44 L), drop-wise. The reaction was allowed to stir at ambient temperature for 72 h, diluted with EtOAc (4 L), washed with 1N HCl (1 L), brine (1 L), the organic layer dried over Na2SO4, filtered and evaporated under reduced pressure. The crude residue was purified by triturating with EtOAc/heptane (1:1/1 L). The slurry was filtered, washed with heptane (2×250 mL) and dried in a vacuum oven at 40° C. for 18 h to afford 470 g of compound 306-C as a white solid. 1H-NMR (DMSO-d6): δ 13.51 (br s, 1H), 10.65 (br s, 1H), 8.12 (d, 2H), 7.86 (d, 2H), 7.83-7.79 (m, 1H), 7.66-7.63 (m, 1H), 7.37-7.33 (m, 1H), 2.03 (s, 3H).

Aufarbeitung

  1. customA 12-L 4-neck flask equipped with an overhead mechanical stirrer, N2 inlet/outlet adapter
  2. washwashed with 1N HCl (1 L), brine (1 L)
  3. dry with materialthe organic layer dried over Na2SO4
  4. filtrationfiltered
  5. customevaporated under reduced pressure
  6. customThe crude residue was purified
  7. customby triturating with EtOAc/heptane (1:1/1 L)
  8. filtrationThe slurry was filtered
  9. washwashed with heptane (2×250 mL)
  10. customdried in a vacuum oven at 40° C. for 18 h

Quellen und Nachweise

ORD-Eintrag
ord-64bc97dbf73749999ebe68314798e32e
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434711B2

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