1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86656249, Verbindung
Reaktionsgleichung
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[C:15]2[CH:16]=[N:17][S:18][C:14]=2[CH:13]=[CH:12][C:11]=1[C:19]([OH:21])=O.C(N(C(C)C)CC)(C)C.C1C=CC2[N:39]([OH:40])N=NC=2C=1.[CH3:41][C:42]1([CH3:50])[O:46][C@H:45]([CH2:47]NO)[CH2:44][O:43]1.CCN=C=NCCCN(C)C>CN(C=O)C.C(OCC)(=O)C>[CH3:50][C:42]1([CH3:41])[O:46][C@@H:45]([CH2:47][O:40][NH:39][C:19]([C:11]2[CH:12]=[CH:13][C:14]3[S:18][N:17]=[CH:16][C:15]=3[C:10]=2[NH:9][C:3]2[CH:4]=[CH:5][C:6]([I:8])=[CH:7][C:2]=2[F:1])=[O:21])[CH2:44][O:43]1Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of 4-(2-fluoro-4-iodo-phenylamino)-benzo[d]iso-thiazole-5-carboxylic acid (250 mg, 0.604 mmol), diisopropylethylamine (0.42 mL, 2.42 mmol), HOBt (163 mg, 0.1.21 mmol) and O—(((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-hydroxylamine (178 mg, 1.21 mmol) in DMF (2 mL) was added EDCI (232 mg, 1.21 mmol). The reaction mixture was stirred for 16 hours at room temperature, diluted with ethyl acetate, and washed with water, a saturated aqueous solution of sodium hydrogen carbonate, then brine before being dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was subjected to flash chromatography (Si—PPC, gradient 0% to 50%, EtOAc in cyclohexane) to afford the title compound as a solid (142 mg, 43%). LCMS (method B): RT=3.92 min, [M+H]+=544.
Aufarbeitung
- washwashed with water
- dry with materiala saturated aqueous solution of sodium hydrogen carbonate, then brine before being dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-7fcc68027f4c4030b17169ff07a82d27
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08841462B2
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