Water → HCID 178487698, compound
Reaction equation
Br[C:2]1[N:3]=[C:4]([C:7]2[CH:16]=[C:15]([OH:17])[C:14]3[C:9](=[C:10]([Cl:20])[C:11]([O:18][CH3:19])=[CH:12][CH:13]=3)[N:8]=2)[S:5][CH:6]=1.O.C[C:23]([N:25](C)C)=O>[Zn].[C-]#N.[C-]#N.[Zn+2].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].C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.[Fe+2]>[Cl:20][C:10]1[C:11]([O:18][CH3:19])=[CH:12][CH:13]=[C:14]2[C:9]=1[N:8]=[C:7]([C:4]1[S:5][CH:6]=[C:2]([C:23]#[N:25])[N:3]=1)[CH:16]=[C:15]2[OH:17]Participants
8
Reactant 3
Product 1
Reagents, catalysts & solvents 4
Procedure
The compound 262 (286 mg, 1 eq.) in degazed dimethylacetamide (10 mL), and Zn (4.5 mg, 0.09 eq.), Zn(CN)2 (84 mg, 0.6 eq.), Pd2dba3 (21 mg, 0.03 eq.), and dppf (26 mg, 0.06 eq.) were heated at 110° C. under microwaves for 30 min. Then, water was added, the precipitate filtered and dissolved in ethyl acetate, dried, and concentrated under vacuum. The residue was purified by chromatography on a silica gel to give compound 263 as a yellow solid in 81% yield. 1H NMR (CDCl3, 400 MHz) δ (ppm) 4.07 (s, 3H), 6.79 (br s, 1H), 7.08 (d, J=9.11 Hz, 1H), 8.19 (s, 1H), 8.28 (d, J=9.11 Hz, 1H), 9.74 (br s, 1H); MS (ESI, EI+): m/z=318.15 (MH+).
Workup
- filtrationthe precipitate filtered
- dissolutiondissolved in ethyl acetate
- customdried
- concentrationconcentrated under vacuum
- customThe residue was purified by chromatography on a silica gel
Sources & evidence
- ORD record
- ord-d6266af399e94643920e9aa3254da276
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09284307B2
Reaction notes
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