Binap, (A+-)- → HCID 24947969, compound
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[NH:7][N:6]=[C:5]2[Cl:13].[CH3:14][N:15]1[CH2:21][CH2:20][CH2:19][N:18]([C:22]2[CH:23]=[C:24]([CH:27]=[CH:28][CH:29]=2)[CH2:25][NH2:26])[CH2:17][CH2:16]1.C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1.CC([O-])(C)C.[Na+]>CC(N(C)C)=O.CCOC(C)=O.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[Cl:13][C:5]1[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([NH:26][CH2:25][C:24]3[CH:27]=[CH:28][CH:29]=[C:22]([N:18]4[CH2:19][CH2:20][CH2:21][N:15]([CH3:14])[CH2:16][CH2:17]4)[CH:23]=3)[CH:3]=2)[C:8](=[O:12])[NH:7][N:6]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (100 mg, 0.385 mmol), 3-(4-methyl-[1,4]diazepan-1-yl)-benzylamine (112 mg, 0.654 mmol), Pd2(dba)3 (53 mg, 0.0578 mmol), rac-BINAP (108 mg, 0.173 mmol) and NaOtBu (139 mg, 1.445 mmol) in DMA (5 mL) was heated at 85° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc and washed with water. The organic layer was washed with sat.aq. NaHCO3, brine and dried (Na2SO4). Preparatory HPLC afforded 4-chloro-6-[3-(4-methyl-[1,4]diazepan-1-yl)-benzylamino]-2H-phthalazin-1-one hydroformate (29 mg) as a pale brown solid. 1H (400 MHz, d6-DMSO) δ: 1.83 (m, 2H), 2.21 (s, 3H). 2.39 (m, 2H), 2.54 (m, 2H), 3.38 (m, 2H), 3.46 (m, 2H), 4.32 (d, 2H), 6.56 (m, 2H), 6.71 (s, 1H), 6.83 (s, 1H), 7.09 (t, 1H), 7.16 (dd, 1H), 7.61 (m, 1H), 7.90 (d, 1H), 8.19 (s, 1H), 12.33 (s, 1H) ppm; m/z (M+1) 398.04.
Workup
- temperatureto cool
- washwashed with water
- washThe organic layer was washed with sat.aq
- dry with materialNaHCO3, brine and dried (Na2SO4)
Sources & evidence
- ORD record
- ord-c2fbc2e7f577404c8a71454411df7aa4
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08044041B2
Reaction notes
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