Diisopropylethylamine → HCID 86650401, compound
Reaction equation
CCN(C(C)C)C(C)C.[CH3:10][O:11][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:21]=1[O:20][C:19](=[O:22])[C:18]([C:23]([OH:25])=O)=[CH:17]2.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH3:50][O:51][C:52]1[CH:53]=[C:54]2[C:59](=[CH:60][CH:61]=1)[CH:58]=[C:57]([C:62]1[CH:63]=[C:64]([NH2:68])[CH:65]=[CH:66][CH:67]=1)[CH:56]=[CH:55]2>CN(C=O)C>[CH3:50][O:51][C:52]1[CH:53]=[C:54]2[C:59](=[CH:60][CH:61]=1)[CH:58]=[C:57]([C:62]1[CH:63]=[C:64]([NH:68][C:23]([C:18]3[C:19](=[O:22])[O:20][C:21]4[C:16]([CH:17]=3)=[CH:15][CH:14]=[CH:13][C:12]=4[O:11][CH3:10])=[O:25])[CH:65]=[CH:66][CH:67]=1)[CH:56]=[CH:55]2Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
DIEA (0.0115 mL, 0.067 mmol) was added to 8-methoxy-3-carboxy-coumarin (0.013 g, 0.06 mmol) and HATU (0.025 g, 0.067 mmol) in 0.5 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 3-(6-methoxy-naphthalen-2-yl)-phenylamine (0.015 g, 0.06 mmol) was added and allowed to react overnight when a solid precipitated out of solution. The resulting precipitate was filtered, dried under suction, and finally dried overnight in vacuo to give 0.023 g of product in 83% yield: LCMS (ESI) m/z 452 (MH+).
Workup
- customresulted
- customto react overnight when a solid
- customprecipitated out of solution
- filtrationThe resulting precipitate was filtered
- customdried under suction, and finally dried overnight in vacuo
Sources & evidence
- ORD record
- ord-1992079fed264437bcb407eed87bd1f8
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642788B2
Reaction notes
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