HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506021Generated: October 29, 2026
Sodium bis(trimethylsilyl)amide → 3-Bromo-6-fluoro-9H-dipyrido[2,3-b;4',3'-d]pyrrole
https://huagongshe.com/reaction/1506021
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 5-Bromo-2,6'-difluoro-[3,4]bipyridinyl-3'-ylamine | HCID 58266654 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-6-fluoro-9H-dipyrido[2,3-b;4',3'-d]pyrrole | HCID 58266831 | — |
Reaction Steps
A solution of 5-bromo-2,6′-difluoro-[3,4′]bipyridinyl-3′-ylamine (0.79 g, 2.76 mmol) in THF (15 mL) was added dropwise over 10 minutes to sodium bis(trimethylsilyl)amide (1N solution in THF, 5.5 mL, 5.52 mmol). The reaction mixture was left to stir for 20 minutes then quenched by the addition of water (2 mL). The resultant black solution was partitioned between ethyl acetate (75 mL) and water (50 mL) and the layers separated. The organic phase was dried over sodium sulfate, filtered and evaporated in vacuo to give an off white solid. The resultant solid was triturated with ethyl acetate (30 mL), collected by filtration, washed with diethyl ether (5 mL) and left to air dry to afford the title compound as an off white solid (0.51 g, 65%). 1H NMR (DMSO-D6, 300 MHz): 9.00 (d, J=2.3 Hz, 1H), 8.69 (d, J=2.3 Hz, 1H), 8.51 (dd, J=1.7, 0.9 Hz, 1H), 7.95 (dd, J=2.4, 0.9 Hz, 1H). LCMS (Method B): RT=3.10 min, M+H+=266/268.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216980B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-039fb25c5e0e40c1ba8c12571f9e6fb0 |
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| Source note | uspto-grants-2015_12 |
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