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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodo-3-methoxypyridineHCID 817173—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
ReactantSodium t-butoxideHCID 23676156—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
SolventTolueneHCID 1140—
Product4-(3-Methoxypyridin-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl esterHCID 59366208—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853202B2
Source datasetuspto-grants-2014_10
ORD IDord-c19f8b2708c24170a3db4ad51240f2e4
Source noteuspto-grants-2014_10