HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184760Generated: November 2, 2026
4-(Tributylstannyl)pyridazine → HCID 67977266, compound
https://huagongshe.com/reaction/1184760
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Tributylstannyl)pyridazine | HCID 6409733 | — |
| Reactant | 4-(5-Chloro-2,3-dihydrofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl ester | HCID 86674895 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67977266 | HCID 67977266 | — |
Reaction Steps
A mixture of 4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (50 mg) and 4-(tributylstannyl)pyridazine (60 mg) in N,N-dimethylformamide (1 mL) is sparged with argon for 10 min and Pd(PPh3)3 (16 mg) is added. The resulting mixture is heated in an oil bath to 120° C. for 7 h. Ethyl acetate and water are added and the organic phase is separated, dried over MgSO4, and concentrated in vacuo. The residue is chromatographed on silica gel (dichloromethane/methanol 95:5→90:10). The crude product is triturated with diethyl ether, filtered off, and dried to give the title compound. LC (method 7): tR=1.35 min; Mass spectrum (ESI+): m/z=383 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669271B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-27e599dd1c0b46c0b65e84ed95271598 |
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| Source note | uspto-grants-2014_03 |
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