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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299288Generated: October 30, 2026

Propargyl alcohol → HCID 178522937, compound

https://huagongshe.com/reaction/2299288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantHCID 178522942HCID 178522942—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
ProductHCID 178522937HCID 17852293720%

Reaction Steps

To a suspension of N-(4-chlorobenzyl)-4-hydroxy-2-iodothieno[2,3-b]pyridine-5-carboxamide (Example No. 2) (1.00 g) in diethylamine (28 mL) is added copper iodide (0.128 g) and Pd(PPh3)2Cl2 (0.032 g) followed by addition of propargyl alcohol (0.16 mL). The reaction is stirred at rt for 3 d. The reaction mixture is partitioned between H2O (100 mL) and ethyl acetate (100 mL). The organic layer is removed, and the aqueous layer is extracted with ethyl acetate (2×100 mL). Combined organic layers are washed with a saturated aqueous NH4Cl solution, dried with MgSO4, filtered, and concentrated in vacuo. The resulting orange solid is purified via column chromatography (CH2Cl2:CH3OH; 98:2, 95:5). Fractions homogeneous by TLC are combined and concentrated in vacuo to yield a pale orange solid which is recrystallized from CH2Cl2/CH3OH to yield 0.165 g (20%) of the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495683B2
Source datasetuspto-grants-2002_12
ORD IDord-84502238766a4efa9a41017698172c7b
Source noteuspto-grants-2002_12