Diethylamine → 7-Acetamido-N,N-diethyl-9-oxo-9H-xanthene-3-carboxamide

HRID 1803348Notes

Reaction equation

HRID 1803348 reaction equation
[C:1]([NH:4][C:5]1[CH:18]=[C:17]2[C:8]([O:9][C:10]3[CH:11]=C(C(O)=O)[CH:13]=[CH:14][C:15]=3[C:16]2=[O:19])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].CN(C([O:30]N1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(NCC)C.[CH:52]([N:55]([CH:58]([CH3:60])C)[CH2:56][CH3:57])([CH3:54])C>CN(C=O)C.O>[CH2:58]([N:55]([CH2:56][CH3:57])[C:52]([C:54]1[CH:13]=[CH:14][C:15]2[C:16](=[O:19])[C:17]3[C:8]([O:9][C:10]=2[CH:11]=1)=[CH:7][CH:6]=[C:5]([NH:4][C:1](=[O:3])[CH3:2])[CH:18]=3)=[O:30])[CH3:60]

Participants

7

Procedure

Compound 6f (2 g, 6.7 mmol) in 35 mL of DMF was treated with HATU (2.5 g, 6.7 mmol), diethylamine (0.2 mL, 8.7 mmol), and diisopropylethylamine (4.75 mL, 26.8 mmol). After stirring for 3 h the reaction was poured into water and the solid was collected to give the product, compound 7f. The filtrate was extracted with diethyl ether/THF (1:1). The combined organic phases were washed with water, brine, and dried over magnesium sulfate. The solvent was evaporated in vacuo and combined with the above solid to give 1.5 g total of compound 7f. MS m/z=353 (M+1).

Workup

  1. customthe solid was collected

Sources & evidence

ORD record
ord-55932a51a8b54378b7218451092db5ea
Source dataset
uspto-grants-2013_01
Patent number
US08350041B2

Reaction notes

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