HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076549Generated: October 28, 2026
N-Iodosuccinimide → HCID 178501068, compound
https://huagongshe.com/reaction/2076549
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 178501056 | HCID 178501056 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178501068 | HCID 178501068 | 79.9% |
Reaction Steps
A solution of methyl trans-4-(2-amino-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-7-yl)cyclohexanecarboxylate (0.200 g, 0.000686 mol) and N-iodosuccinimide (0.278 g, 0.00124 mol) in anhydrous DMF (4.0 mL) was stirred at rt for 48 h. The reaction was concentrated in vacuo then partitioned between H2O and EtOAc. The aqueous material was re-extracted with EtOAc (3×) and the combined organic fractions were washed with H2O (2×), Na2S2O3 (2×) and brine (1×). The aqueous was re-extracted with CHCl3 and combined with the EtOAc fractions dried over Na2SO4, filtered and concentrated in vacuo resulting in 229 mg, (79.9% yield) of the title compound as a light orange solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.34-1.65 (m, 4H), 1.88-2.06 (m, 4H), 2.33-2.45 (m, 1H), 2.91-3.01 (m, 1H), 3.61 (s, 3H), 6.17 (s, 2H) and 10.82 (br. s., 1H); MS (ES+): m/z 417.82 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07923555B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-89eb3df63a2046da9a3a4b3bf8556921 |
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| Source note | uspto-grants-2011_04 |
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