Sodium Sulfate → Bms-587101

HRID 1792876Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1792876
[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13](=[O:14])[C@@:12]3([C@H:18]([C:19]4[CH:26]=[CH:25][C:22]([C:23]#[N:24])=[CH:21][CH:20]=4)[CH2:17][NH:16][CH2:15]3)[N:11]([CH3:27])[C:10]2=[O:28])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[CH:29]([C:31]1[S:35][CH:34]=[C:33]([C:36]([OH:38])=[O:37])[CH:32]=1)=O.S([O-])([O-])(=O)=O.[Na+].[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl>[C:23]([C:22]1[CH:21]=[CH:20][C:19]([C@H:18]2[C@:12]3([N:11]([CH3:27])[C:10](=[O:28])[N:9]([C:4]4[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([Cl:1])[CH:3]=4)[C:13]3=[O:14])[CH2:15][N:16]([CH2:29][C:31]3[S:35][CH:34]=[C:33]([C:36]([OH:38])=[O:37])[CH:32]=3)[CH2:17]2)=[CH:26][CH:25]=1)#[N:24]

Komponenten

6

Edukt 4

HCID 24436Sodium SulfateHCID 8188835-Formylthiophene-3-carboxylic acidHCID 5049666Sodium triacetoxyborohydrideHCID 119947544-[(5S,9R)-3-(3,5-Dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non-9-yl]-benzonitrile

Produkt 1

HCID 11635371Bms-587101Ausbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 111,2-DichloroethaneLösungsmittel

Versuchsvorschrift

To a solution of 4-[(5S,9R)-3-(3,5-Dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non-9-yl]-benzonitrile (0.1 g, 0.24 mmol) (Example 15a) in 1,2-DCE (4 mL) were sequentially added 5-Formyl-3-thiophenecarboxylic acid (0.045 g, 0.29 mmol) and sodium sulfate (150 mgs) under a nitrogen atmosphere at room temperature. The contents were stirred at room temperature for twenty hours and sodium triacetoxyborohydride (0.075 g, 0.336 mmol) was added. The reaction was allowed to continue at room temperature for six hours and quenched by the addition of water (15 m]L). DCM (15 mL) was added, and sulfurdioxide gas was bubbled through the reaction mixture for ten minutes and the contents transferred into a separating funnel. The organic layer was separated, washed with brine (2×20 μL), dried over sodium sulfate, concentrated under reduced pressure and purified by silica gel column chromatography using DCM and MeOH to yield 0.1 g of the titled compound. Retention time: 3.09 min. YMC S5 Combiscreen 4.6×50 mm (4 minute gradient). Solvent A=10% MeOH, 90% water and 0.2% phosphoric acid. Solvent B=90% MeOH, 10% water and 0.2% phosphoric acid.

Aufarbeitung

  1. customat room temperature
  2. customquenched by the addition of water (15 m]L)
  3. additionDCM (15 mL) was added
  4. customsulfurdioxide gas was bubbled through the reaction mixture for ten minutes
  5. customthe contents transferred into a separating funnel
  6. customThe organic layer was separated
  7. washwashed with brine (2×20 μL)
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated under reduced pressure
  10. custompurified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-35aad3b2b74b4113a221a93457d4b0e4
Quelldatensatz
uspto-grants-2006_07
Patentnummer
US07078420B2

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