Sodium Iodide → (2S,3S,5R)-4-[5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxymethoxycarbonyl]-2-(3,5-difluorophenyl)-3,5-dimethyl-2-morpholinol

HRID 2357759Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2357759
Cl[CH2:2][O:3][C:4]([N:6]1[C@H:11]([CH3:12])[CH2:10][O:9][C@:8]([C:14]2[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([F:21])[CH:15]=2)([OH:13])[C@@H:7]1[CH3:22])=[O:5].[CH:23]1[CH:24]=[C:25]([CH2:28][NH:29][C:30]2[C:35]([C:36]([OH:38])=[O:37])=[CH:34][C:33]([S:39]([NH2:42])(=[O:41])=[O:40])=[C:32]([Cl:43])[CH:31]=2)[O:26][CH:27]=1.[Cs].[I-].[Na+].CCCCCCC>O1CCCC1.C(OCC)(=O)C>[NH2:42][S:39]([C:33]1[C:32]([Cl:43])=[CH:31][C:30]([NH:29][CH2:28][C:25]2[O:26][CH:27]=[CH:23][CH:24]=2)=[C:35]([CH:34]=1)[C:36]([O:38][CH2:2][O:3][C:4]([N:6]1[C@H:11]([CH3:12])[CH2:10][O:9][C@:8]([C:14]2[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([F:21])[CH:15]=2)([OH:13])[C@@H:7]1[CH3:22])=[O:5])=[O:37])(=[O:41])=[O:40]

Komponenten

7

Edukt 4

HCID 5238Sodium IodideHCID 8900HeptaneHCID 59613210(2S,3S,5R)-2-(3,5-difluorophenyl)-2-hydroxy-3,5-dimethylmorpholine-4-carboxylic acid chloromethyl esterHCID 86613437Furosemide cesium

Produkt 1

HCID 16214883(2S,3S,5R)-4-[5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxymethoxycarbonyl]-2-(3,5-difluorophenyl)-3,5-dimethyl-2-morpholinolAusbeute 13,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a stirring solution of (2S,3S,5R)-2-(3,5-difluorophenyl)-2-hydroxy-3,5-dimethylmorpholine-4-carboxylic acid chloromethyl ester (1410) (2.24 g, 6.67 mmol) in 150 mL of anhydrous tetrahydrofuran was added the furosemide cesium salt (10c) (3.09 gm, 6.67 mmol) and sodium iodide (1.10 gm, 7.34 mmol). The mixture was heated to ˜60° C. and monitored by TLC (1:1 heptane:ethyl acetate). After heating for 6 hours, TLC analysis indicated a slowing down of product formation with starting materials remaining. The reaction was halted so as not to allow by-product formation. The solvent was removed from the crude yellow mixture, and it was dried onto silica gel. This crude material was purified on an Optix Companion Automated Chromatography system using an 80 gm silica cartridge and eluting with ethyl acetate/heptane (0 to 70% over 50 minutes). This material was dried on a vacuum pump for 24 hours and afforded 0.560 g of (2S,3S,5R)-4-[5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxymethoxycarbonyl]-2-(3,5-difluorophenyl)-3,5-dimethyl-2-morpholinol (1420) as a light yellow foamy solid. Melting point range was 105° C. to 110° C. Elemental analysis calculated for [C26H26N3 0.3 EtOAc]: C, 49.76; H, 4.36; N, 6.4. found C, 50.08; H, 4.65; N, 6.23. 1H NMR (400 MHz, CDCl3) δ 0.86-0.89 (t, 3H), 1.34 (m, 3H), 3.60-3.67 (m, 1H), 4.23 (m, 1H), 4.33 (m, 1H), 4.45-4.46 (d, 2H), 4.47 (s, 1H), 5.07-5.11 (d, 2H), 6.00-6.05 (dd, 2H), 6.28 (s, 1H), 6.35 (s, 1H), 6.75-6.79 (t, 1H), 6.89 (m, 1H), 7.12-7.14 (br. d, 2H), 7.37-7.39 (d, 1H), 8.53 (br. d., 1H), 8.63 (s, 1H).

Aufarbeitung

  1. temperatureAfter heating for 6 hours
  2. customThe solvent was removed from the crude yellow mixture, and it
  3. customwas dried onto silica gel
  4. customThis crude material was purified on an Optix Companion Automated Chromatography system
  5. washeluting with ethyl acetate/heptane (0 to 70% over 50 minutes)
  6. customThis material was dried on a vacuum pump for 24 hours

Quellen und Nachweise

ORD-Eintrag
ord-c0cdc877811d4c418151490d3ae1b264
Quelldatensatz
uspto-grants-2010_07
Patentnummer
US07763612B2

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