HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655931Generated: November 1, 2026
Dimethylformamide → HCID 57425159, compound
https://huagongshe.com/reaction/655931
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | 5-Fluoro-1H-indazole-7-carboxamide | HCID 57425163 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57425159 | HCID 57425159 | — |
Reaction Steps
To a solution of D2 (1.0 eq) in DMF (0.2 M) K2CO3 (1.3 eq) and 4-bromofluorobenzene (10.0 eq) were added and the reaction mixture was heated under MW conditions at 180° C. for 20 min. The reaction mixture was cooled to RT and diluted with EtOAc. The organic phase was washed with brine; dried (Na2SO4). Evaporation of the solvent gave (D3) which was purified by chromatography on silica gel eluting with 50-70% EtOAc/Petroleum ether to obtain the title compound as a yellow powder. 1H NMR (400 MHz, DMSO-d6, 300K) δ 9.34 (1H, s), 8.50 (1H, br. s), 8.17 (2H, d, J=9.0 Hz), 8.03 (1H, br. s), 7.90-7.80 (4H, m). MS (ES+) C14H9BrFN3O requires: 334/336. Found: 335/337 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071623B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-c073adb2f40e41bbba19d77f22b97c3e |
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| Source note | uspto-grants-2011_12 |
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