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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825070Generated: November 3, 2026

7-Chloro-2-iodothieno(3,2-b)pyridine → HCID 22143687, compound

https://huagongshe.com/reaction/1825070

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-2-iodothieno(3,2-b)pyridineHCID 17750400—
ReactantHCID 22143620HCID 22143620—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventO-XyleneHCID 7237—
ProductHCID 22143687HCID 22143687—

Reaction Steps

A mixture of 1-methyl-5-trimethylstannanyl-1H-pyrazole 10a (2.1 g, 8.5 mmole), 7-chloro-2-iodo-thieno[3,2-b]pyridine (2.5 g, 8.5 mmole), tetrakis(triphenylphosphine)palladium(0) (0.5 g, 0.4 mmole, 5 mol %) in o-xylene (85 ml was degassed, purged with nitrogen and heated to 120°, which gave an orange solution. After 14 hours the black reaction mixture was diluted with toluene (100 ml) and extracted with 1.2 M HCl (3×60 ml). The combined aqueous layers were washed with toluene (100 ml). The organic layers were discarded and the aqueous layer was treated with NaOH to pH 14. The resultant white solid was collected (1.1 g, 52%): TLC (6% methanol-dichloromethane) Rf 0.8; 1H-NMR (DMSO-d6, 400 MHz) δ 8.70 (1H, d, J=5.3 Hz), 8.00 (1H, s), 7.63 (1H,d, J=5.3 Hz), 7.56 (1H, d, J=2.0 Hz), 6.79 (1H, d, J=2.0 Hz), 4.09 (3H, s). ESIMS m/z 250 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045528B2
Source datasetuspto-grants-2006_05
ORD IDord-5274bedf59ad469fa9832c943327270e
Source noteuspto-grants-2006_05