HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870742Generated: November 1, 2026
N-Iodosuccinimide → HCID 86696450, compound
https://huagongshe.com/reaction/870742
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 86696451 | HCID 86696451 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86696450 | HCID 86696450 | — |
Reaction Steps
A solution of 4-imidazo[1,2-b]pyridazin-6-yl-piperazine-1-carboxylic acid tert-butyl ester (3.6 g, 11.8 mmol) and N-iodosuccinimide [516-12-1] (3.1 g, 13.1 mmol) in DMF (120 mL) was stirred under N2 blanket at ambient temperature for 2 h then partitioned between 5% (w/v) aqueous sodium metabisulfite and ethyl acetate. The organic phase was washed with brine, dried (CaSO4), evaporated, and crystallized from ethyl acetate/heptane to provide a white crystalline powder, mp. 203-204° C. (dec.). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.43 (s, 9H) 3.45-3.51 (m, 4H) 3.51-3.58 (m, 4H) 7.19 (d, J=9.92 Hz, 1H) 7.61 (s, 1H) 7.85 (d, J=9.92 Hz, 1H). 13C NMR (100 MHz, DMSO-d6) δ ppm 27.89, 45.06, 70.52, 78.95, 110.55, 125.66, 137.28, 137.71, 153.73, 154.88. LRMS (ESI) m/z 430.0 (M+H)]+, calc'd for C15H20IN5O2: 429.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969565B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-25754b0a1468446ba803f4b0e5369cca |
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| Source note | uspto-grants-2015_03 |
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