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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099289Generated: November 1, 2026

Sodium Iodide → HCID 59231977, compound

https://huagongshe.com/reaction/1099289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 59232069HCID 59232069—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59231977HCID 5923197725%

Reaction Steps

To a solution of 2-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)ethanol (440 mg, 2.5 mmol) in THF (10 ml) and CH2Cl2 anhydrous (10 ml) and was added SOCl2 (0.36 ml, 4.9 mmol) and stirred at rt. After 20 min all starting material was consumed. The crude reaction mixture was concentrated in vacuo to dryness and was suspended in dry CH2Cl2. The solvent was evaporated and the crude was re-suspended in CH2Cl2 and concentrated in vacuo to dryness. The resulting solid was dissolved in DMF (10 ml) and was added triethylamine (0.97 ml, 7.2 mmol), morpholine (1.0 ml, 11.7 mmol) and NaI (280 mg, 1.87 mmol) and heated at 55° C. 24 h. Cooled to rt, the reaction crude was diluted with EtOAc (30 ml) and washed with H2O (2×) and brine (2×), dried over Na2SO4 and concentrated to give yellow solid. The crude was purified by MPLC with 0-10% MeOH/CH2Cl2 to give 149 mg of the titled compound (yield 25%). MS [M+H]+=248; LCMS RT=1.05 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143393B2
Source datasetuspto-grants-2012_03
ORD IDord-4f97674947c749b784a138f8359035ab
Source noteuspto-grants-2012_03