HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749039Generated: October 28, 2026
Potassium tert-butoxide → HCID 22347175, compound
https://huagongshe.com/reaction/749039
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178514377 | HCID 178514377 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 22347175 | HCID 22347175 | 25.6% |
Reaction Steps
To a solution of N1-(4-bromophenyl)-2-fluoro-1-benzenecarbohydrazonamide (1.2 g, 0.00391 mol) in N-methyl pyrrolidinone (25 mL), potassium tert-butoxide (0.50 g, 0.0041 mol) was added and the resulting solution was heated at 100° C. under an atmosphere of nitrogen for 3 hours. The reaction mixture was cooled to ambient temperature, the solvent was removed under reduced pressure and the residue partitioned between saturated solution of sodium bicarbonate in water (50 mL) and ethyl acetate (50 mL). The organic phase was washed with brine, dried with magnesium sulfate and concentrated. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (1:5) as mobile phase to yield N-(4-bromophenyl)-N-(1H-3-indazolyl)amine (0.29 g, 0.0010 mol) as a white solid. 1H NMR (DMSO-d6, 400 MHz), δ 12.06 (s, 1H), 9.03 (s, 1H), 7.93 (d, 1H), 7.65 (d, 2H), 7.35 (m, 4H), 7.03 (dd, 1H). TLC (ethyl acetate/heptane 1:3) Rf 0.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07400979B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-5debf509905a43c38616fb202dd6ba2f |
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| Source note | uspto-grants-2008_07 |
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