HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532813Generated: October 29, 2026
2-Iodo-3-methoxypyridine → 4-(3-Methoxypyridin-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/532813
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodo-3-methoxypyridine | HCID 817173 | — |
| Reactant | Tert-butyl 1,4-diazepane-1-carboxylate | HCID 2756058 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(3-Methoxypyridin-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester | HCID 59366208 | — |
Reaction Steps
Toluene (1.5 mL) was added to a mixture of 2-iodo-3-methoxypyridine (350 mg, 1.49 mmol), BOC-homopiperazine (0.410 mL, 2.09 mL), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (26 mg, 0.07 mmol), and trisdibenzylideneacetone dipalladium (20 mg, 0.02 mmol). To this suspension was added sodium t-butoxide (201 mg, 2.09 mmol) and the mixture was heated to 65° C. for 15 h. The mixture was filtered through celite, and the filter cake was washed with EtOAc. The resulting solution was washed with H2O, then brine, and dried over MgSO4. After removal of the solvent, the residue was purified on silica to give 335 mg of the title compound as a dark oil. MS (ES) m/z 308 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853202B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c19f8b2708c24170a3db4ad51240f2e4 |
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| Source note | uspto-grants-2014_10 |
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