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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237153Generated: October 31, 2026

Methanol → HCID 68436311, compound

https://huagongshe.com/reaction/2237153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant3-MethoxypropyneHCID 69393—
ReactantHCID 15539884HCID 15539884—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68436311HCID 68436311—

Reaction Steps

To a mixture of 4,6-diamino-1-(2-deoxy-β-D-erythro-pentofuranosyl)-3-iodo-1H-pyrazolo[3,4-d]pyrimidine (4.2 g, 10.71 mmol), CuI (211 mg, 1.10 mmol), Pd(PPh3)4 (635 mg, 0.553 mmol), and triethylamine (2.2 mL) in 20 mL of anhydrous DMF was added methyl propargyl ether (1.82 mL). The mixture was stirred under argon for 16 h. and then evaporated to dryness. The residue was crystallized from methanol: 3.20 g (89%) yield; TLC (30% methanol in ethyl acetate), Rf=0.63; 1H NMR (DMSO-d6) δ 7.44 (2H, br d, amino), 6.32 (1H, t, J=6.6 Hz, 1′-H), 6.33 (2H, br s, amino), 5.20 (1H, d, J=4.1 Hz, 3′-OH), 4.75 (1H, br t, 5′-OH), 4.40 (2H, s, methylene), 4.36 (1H, m, 3′-H), 3.76 (1H, m, 4′-H), 3.47 & 3.32 (2H, 2×m, 5′-Hs), 3.32 (3H, s, methoxy), 2.68 & 2.14 (2H, 2×m, 2′-Hs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07715989B2
Source datasetuspto-grants-2010_05
ORD IDord-f469aa4c32eb4c0d82aec3600095c784
Source noteuspto-grants-2010_05