HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803535Generated: October 25, 2026
2-Fluoro-5-(trifluoromethyl)benzylamine → 4-Chloro-6-(2-fluoro-5-trifluoromethyl-benzylamino)-2H-phthalazin-1-one
https://huagongshe.com/reaction/1803535
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluoro-5-(trifluoromethyl)benzylamine | HCID 533839 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 6-Bromo-4-chlorophthalazin-1(2H)-one | HCID 53308487 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-Chloro-6-(2-fluoro-5-trifluoromethyl-benzylamino)-2H-phthalazin-1-one | HCID 58447231 | — |
Reaction Steps
A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2-fluoro-5-trifluoromethyl-benzylamine (124 mg, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (132 mg, 0.17 mmol) and NaOt-Bu (140 mg, 1.45 mmol) in DMA (6 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-(2-fluoro-5-trifluoromethyl-benzylamino)-2H-phthalazin-1-one: 27 mg (12.5%): m/z (M+H)=372. 1H-NMR (DMSO-d6) δ: 12.38 (s, 1H), 7.95 (d, 1H), 7.85 (m, 1H), 7.75 (m, 1H), 7.65 (m, 1H), 7.49 (m, 1H), 7.19 (dd, 1H), 6.87 (s, 1H), 4.56 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349836B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ea1da6fa572e4486aeb90ce755eec1b6 |
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| Source note | uspto-grants-2013_01 |
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