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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661940Generated: November 1, 2026

Triacetoxyperiodinane → HCID 86642952, compound

https://huagongshe.com/reaction/661940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 59375141HCID 59375141—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86642952HCID 8664295285.2%

Reaction Steps

Step 1 A solution of 4-(3-(4-fluorobenzamido)-2-methylphenyl)-7-(hydroxymethyl)-9H-carbazole-1-carboxamide (Example 31-4, 0.54 g, 1.155 mmol) in THF (38.5 mL) was treated with 1,1,1-tris(acetyloxy)-1,1-dihydro-1,2-benziodoxol-3-(1H)-one (Dess-Martin periodinane, 0.784 g, 1.848 mmol) at rt and the mixture was stirred for 2 h. The mixture was partitioned between NaHCO3 (aq) and EtOAc. The organic phase was washed with brine, dried and concentrated. The residue was triturated with methanol and the solid was collected by filtration and dried to provide 4-(3-(4-fluorobenzamido)-2-methylphenyl)-7-formyl-9H-carbazole-1-carboxamide as an orange solid (458 mg, 85%). 1H NMR (400 MHz, DMSO-d6) δ 11.98 (1H, s), 10.16 (1H, s), 10.03 (1H, s), 8.23-8.32 (2H, m), 8.05-8.14 (3H, m), 7.60 (1H, br. s.), 7.49-7.55 (1H, m), 7.39-7.49 (2H, m), 7.32-7.39 (2H, m), 7.21-7.27 (1H, m), 7.09 (2H, t, J=8.1 Hz), 1.88 (3H, s). Mass spectrum m/z 466.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-c43cd481a34549cdb4223700561359fa
Source noteuspto-grants-2011_12