Diethylamine → N,N-Diethyl-6-methoxy-9-oxo-9H-xanthene-3-carboxamide
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:14](=[CH:15][CH:16]=1)[C:13](=[O:17])[C:12]1[CH:11]=[CH:10][C:9]([C:18](O)=[O:19])=[CH:8][C:7]=1[O:6]2.F[P-](F)(F)(F)(F)F.N1C2C=CC=C(OC(N(C)C)=[N+](C)C)C=2N=N1.[CH:45]([N:48](CC)[CH:49](C)[CH3:50])(C)[CH3:46].C(NCC)C>CN(C)C=O>[CH2:45]([N:48]([CH2:49][CH3:50])[C:18]([C:9]1[CH:10]=[CH:11][C:12]2[C:13](=[O:17])[C:14]3[C:5]([O:6][C:7]=2[CH:8]=1)=[CH:4][C:3]([O:2][CH3:1])=[CH:16][CH:15]=3)=[O:19])[CH3:46]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of compound 6i (0.707 g, 2.62 mmol) and O-benzotriazol-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HBTU, 1.05 g, 2.74 mmol) in N,N-dimethylformamide (10 mL) was treated with N,N-diisopropylethylamine (DIEA, 0.685 mL, 3.92 mmol) and allowed to stir at rt for 15 min. Diethylamine (0.541 mL, 5.23 mL) was added and the resultant mixture was stirred for 2 h. The mixture was poured into ice water. A solid was collected by filtration, washed with water and air dried to give the title compound (0.445 g). MS: m/z 326.0 (MH+). 1H NMR (DMSO-d6): δ 1.07 (br t, 3H), 1.19 (br t, 3H), 3.20 (br q, 2H), 3.48 (br t, 2H), 3.95 (s, 3H), 7.08 (m, 1H), 7.17 (d, 1H, J=2.1 Hz), 7.40 (d of d, 1H, J=1.3 & 8.1 Hz), 7.59 (d, 1H, J=1.2 Hz), 8.12 (d of d, 1H, J=1.3 & 8.9 Hz) and 8.21 (d, 1H, J=8.1 Hz).
Workup
- filtrationA solid was collected by filtration
- washwashed with water and air
- customdried
Sources & evidence
- ORD record
- ord-769ff43f306b402b82c397e0ebc8ab5c
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106207B2
Reaction notes
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