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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350397Generated: October 30, 2026

HCID 23511825, compound → methyl 4-[N-[1-[3-methoxy-4-[N'-(2-fluorophenyl)ureido]phenylacetyl]-2-pyrrolidinyl methyl]-N-methylamino]-3-nitrobenzoate

https://huagongshe.com/reaction/350397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23511825HCID 23511825—
Reactantmethyl 3-nitro-4-[N-(2-pyrrolidinyl)methyl-N-methylamino]benzoateHCID 23511932—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Catalyst1-HydroxybenzotriazoleHCID 75771—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Productmethyl 4-[N-[1-[3-methoxy-4-[N'-(2-fluorophenyl)ureido]phenylacetyl]-2-pyrrolidinyl methyl]-N-methylamino]-3-nitrobenzoateHCID 69332166105.5%

Reaction Steps

A mixture of 3-methoxy-4-[N′-(2-fluorophenyl)ureido]phenylacetic acid (630.0 mg, 1.979 mmol), methyl 3-nitro-4-[N-(2-pyrrolidinyl)methyl-N-methylamino]benzoate (553.0 mg, 1.885 mmol), EDC(Hydrochloride) (542.0 mg, 2.827 mmol), HOBt (25.5 mg, 0.189 mmol), and DMAP (23.1 mg, 0.189 mmol) in DMF (5.0 mL) was stirred at room temp. for 2 hr. The mixture was diluted with Et2O, washed with brine, and dried over Na2SO4. The solvent was removed under a reduced pressure, and the residue was chromatographed on silica-gel with CHCl3-MeOH (30:1, v/v) as eluent to afford 1.18 g (100%) methyl 4-[N-[1-[3-methoxy4-[N′-(2-fluorophenyl)ureido]phenylacetyl]-2-pyrrolidinyl methyl]-N-methylamino]-3-nitrobenzoate as a yellow foam, which is used to the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-fb623a385acd471e8992840f936a25a5
Source noteuspto-grants-2007_02