HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550095Generated: October 30, 2026
N-Iodosuccinimide → HCID 136102521, compound
https://huagongshe.com/reaction/550095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 136102522 | HCID 136102522 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136102521 | HCID 136102521 | — |
Reaction Steps
To a solution of 7-cyclohexylimidazo[5,1-f] [1,2,4]triazin-4(3H)-one (130 mg, 0.6 mmol) in DMF (0.6 mL) was added N-iodosuccinimide (700 mg, 0.003 mol) and the reaction mixture stirred at 55° C. for 20 h. After this time the mixture was diluted with water (50 mL) and extracted with EtOAc (4×40 mL). The organic extracts were washed with water (4×40 mL), treated with sodium thiosulfate and brine, dried over Na2SO4 and concentrated in vacua to afford 7-cyclohexyl-5-iodoimidazo[5,1-f] [1,2,4]triazin-4(3H)-one. 1H NMR (400 MHz-DMSO-d6) δ 1.34-1.37 (m, 3H), 1.52-1.56 (m, 2H), 1.76-1.88 (m, 5H), 3.06-3.08 (m, 1H) 7.87 (s, 1H) 11.78 (s, 1H); MS (ES+): m/z: 344.95 (100) [MH+]. HPLC: tr=2.95 min (OpenLynx: polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943767B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-2de3569b0582466dab78cfb1659d52fb |
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| Source note | uspto-grants-2011_05 |
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