Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875134Generated: October 26, 2026

Iodine → HCID 57444149, compound

https://huagongshe.com/reaction/875134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIsoamyl NitriteHCID 8053—
ReactantCesium iodideHCID 24601—
Reactant8-amino-1-methyl-N-[(1S)-2-morpholin-4-yl-1-phenylethyl]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 57444150—
CatalystCopper iodideHCID 83717—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57444149HCID 5744414940%

Reaction Steps

To a well stirred and warm suspension of 8-amino-1-methyl-N-[(1S)-2-morpholin-4-yl-1-phenylethyl]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (3 g, 6.92 mmol) in dimethoxyethane (240 mL), maintained in an inert atmosphere of argon, cesium iodide (2.16 g, 8.3 mmol), bisublimated iodine (870 mg, 3.46 mmol), copper iodide (460 mg, 2.42 mmol) and isopentyl nitrite (1.71 mL, 1.5 g, 12.46 mmol) were added, in sequence. The reaction mixture was stirred vigorously at 65-70° C. for 18 hours. After cooling in an ice-water bath, the solid was filtered off and the filtrate was diluted with dichloromethane (100 mL), washed with 30% ammonium hydroxide (50 mL), sodium thiosulphate (100 mL), brine and dried over anhydrous Na2SO4. The crude was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95:59) and 1.48 g of the title compound was isolated (40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981089B2
Source datasetuspto-grants-2015_03
ORD IDord-a66929b05d5c46d2b1df2f0d4e403f82
Source noteuspto-grants-2015_03