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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Chloro-2-iodothieno(3,2-b)pyridine | HCID 17750400 | — |
| Reactant | HCID 22143620 | HCID 22143620 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22143687 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045528B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-5274bedf59ad469fa9832c943327270e |
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| Source note | uspto-grants-2006_05 |
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