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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350393Generated: November 1, 2026

Methyl 2-(2-pyrrolidinyl)methoxypyridine-5-carboxylate → HCID 69333525, compound

https://huagongshe.com/reaction/350393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(2-pyrrolidinyl)methoxypyridine-5-carboxylateHCID 23511785—
ReactantHCID 23512521HCID 23512521—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 69333525HCID 69333525—

Reaction Steps

The mixture of pentafluorophenyl 4-[N′-(2-fluorophenyl)ureido]-3-methoxy-phenylacetate (314.8 mg, 0.650 mmol), methyl 2-[(2-pyrrolidinyl)methoxy]pyridine-5-carboxylate (146.2 mg, 0.619 mmol), Et3 N (103 ul, 0.743 mmol) in DMF (1.5 mL) was stirred for 1 hr at room temp. The mixture was diluted with Et2O, washed with brine, and dried over Na2SO4. The solvent was removed under a reduced pressure to afford methyl 2-[[1-[4-[N′-(2-fluorophenyl)ureido]-3-methoxyphenylacetyl]-2-pyrrolidinyl]methoxy]pyridine-5-carboxylate as a crude pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-2ec67ae6fef147d6bbd166cfddf9873a
Source noteuspto-grants-2007_02