1,2-Dichloroethane → (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)-phenyl)-2-(3-(methylsulfonamido)thiophene-2-carbonyloxy)ethyl)pyridine 1-oxide

HRID 59737Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 59737
[CH3:1][S:2]([NH:5][C:6]1[CH:10]=[CH:9][S:8][C:7]=1[C:11]([OH:13])=[O:12])(=[O:4])=[O:3].[Cl:14][C:15]1[CH:16]=[N+:17]([O-:40])[CH:18]=[C:19]([Cl:39])[C:20]=1[CH2:21][C@@H:22]([C:24]1[CH:29]=[CH:28][C:27]([O:30][CH:31]([F:33])[F:32])=[C:26]([O:34][CH2:35][CH:36]2[CH2:38][CH2:37]2)[CH:25]=1)O.C(Cl)CCl>CN(C1C=CN=CC=1)C.C(Cl)Cl>[Cl:14][C:15]1[CH:16]=[N+:17]([O-:40])[CH:18]=[C:19]([Cl:39])[C:20]=1[CH2:21][C@@H:22]([C:24]1[CH:29]=[CH:28][C:27]([O:30][CH:31]([F:33])[F:32])=[C:26]([O:34][CH2:35][CH:36]2[CH2:38][CH2:37]2)[CH:25]=1)[O:12][C:11]([C:7]1[S:8][CH:9]=[CH:10][C:6]=1[NH:5][S:2]([CH3:1])(=[O:3])=[O:4])=[O:13]

Komponenten

6

Versuchsvorschrift

A mixture of 3-(methylsulfonamido)thiophene-2-carboxylic acid (Int. 38) (110 mg, 0.497 mmol), (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)-phenyl)-2-hydroxyethyl)pyridine 1-oxide (209 mg, 0.497 mmol), EDC (286 mg, 1.491 mmol) and DMAP (30.4 mg, 0.249 mmol) in DCM (25 ml) was stirred at RT for 3 days. The mixture was diluted with DCM and washed with 1N HCl and aqueous NaHCO3; the organic layer was dried over Na2SO4, filtered and evaporated. The crude was purified by flash chromatography on silica gel cartridge (DCM/MeOH=99.5/0.5 to 99/1) affording (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)-phenyl)-2-(3-(methylsulfonamido)thiophene-2-carbonyloxy)ethyl)pyridine 1-oxide (Int. 39) (95 mg, 0.152 mmol, MS/ESI+623.05 [MH]+, [αD]=−28.6, c=0.3, DCM).

Aufarbeitung

  1. washwashed with 1N HCl and aqueous NaHCO3
  2. dry with materialthe organic layer was dried over Na2SO4
  3. filtrationfiltered
  4. customevaporated
  5. customThe crude was purified by flash chromatography on silica gel cartridge (DCM/MeOH=99.5/0.5 to 99/1)

Quellen und Nachweise

ORD-Eintrag
ord-242719a229a24142be1434d632b1633f
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09440954B2

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