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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473953Generated: October 25, 2026

Diisopropyl diazene-1,2-dicarboxylate → Methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylate

https://huagongshe.com/reaction/473953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantCyclopentanecarboxylic acid, 3-hydroxy-, methyl esterHCID 520596—
ReactantHCID 178515818HCID 178515818—
SolventTolueneHCID 1140—
ProductMethyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylateHCID 5857790751%

Reaction Steps

A solution of methyl 3-hydroxycyclopentanecarboxylate A-11 (500.0 mg, 3.00 mmol) in anhydrous toluene (10.0 mL) was added to a solution of 5-bromopyridin-2-ol (522.0 mg, 3.00 mmol) in anhydrous toluene (10.0 mL) at room temperature. Diisopropyl azodicarboxylate (1.57 g, 6.00 mmol) was then added dropwise, and the yellow-orange solution was stirred at room temperature for 12 h. The reaction mixture was then quenched with methanol (1.0 mL) and concentrated to dryness under reduced pressure. The residue was purified by flash column chromatography on silica gel (hexanes to ethyl acetate gradient) to give methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylate A-12 (462.0 mg, Yield=51%). MS (ESI), [M+Na]+ 321, 323.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637507B2
Source datasetuspto-grants-2014_01
ORD IDord-9b2e0014adbe449db1634b351e2ff97b
Source noteuspto-grants-2014_01