HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278308Generated: October 30, 2026
Dimethylformamide → 2-(7-methylspiro[2H-benzofuran-3,1'-cyclopropane]-4-yl)oxy-5-nitro-pyridine
https://huagongshe.com/reaction/2278308
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | 7-methylspiro[2H-benzofuran-3,1-cyclopropane]-4-ol | HCID 57411301 | — |
| Product | 2-(7-methylspiro[2H-benzofuran-3,1'-cyclopropane]-4-yl)oxy-5-nitro-pyridine | HCID 67960126 | 90.5% |
Reaction Steps
To a solution of 7-methylspiro[2H-benzofuran-3,1′-cyclopropane]-4-ol (Intermediate 13, 176 mg, 1 mmol) in dry DMF (4 ml) potassium carbonate (207 mg, 1.5 mmol) and then 2-chloro-5-nitropyridine (158 mg, 1 mmol) were added and the reaction mixture was stirred for 2 hours at 80° C. After cooling the reaction mixture was quenched with water (2 ml), diluted with brine (10 ml) and extracted with ethyl acetate (2×20 ml). The organic layer was dried over sodium sulfate, filtered and evaporated affording the title compound (270 mg) as an orange solid that was used in the next step as crude material without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133175B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-8c697b400c794182bfe6ec9634a8b350 |
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| Source note | uspto-grants-2015_09 |
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