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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350559Generated: October 31, 2026

1-Hydroxybenzotriazole → methyl (S)-3-chloro-4-[2-[N-methyl-N-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]amino]-1-propoxy]benzoate

https://huagongshe.com/reaction/350559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Methoxy-4-o-tolylureidophenylacetic acidHCID 11449840—
Reactantmethyl (S)-3-chloro-4-(2-methylamino-1-propoxy)benzoateHCID 86587798—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productmethyl (S)-3-chloro-4-[2-[N-methyl-N-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]amino]-1-propoxy]benzoateHCID 86595082102.2%

Reaction Steps

A mixture of 3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetic acid (261 mg, 0.83 mmol), methyl (S)-3-chloro-4-(2-methylamino-1-propoxy)benzoate (214 mg, 0.83 mmol), EDC(hydrochloride) (239 mg, 1.25 mmol), HOBt (168 mg, 1.24 mmol), and DMAP (20 mg, 0.16 mmol) in DMF (8 mL) was stirred at room temp for 2 hr. The mixture was diluted with EtOAc, washed with 0.5 N HCl, brine, dried over Na2SO4 and evaporated. The residue was purified by column chromatography on silica-gel with CHCl3-MeOH (50:1, v/v) as eluent to give 470 mg (100%) methyl (S)-3-chloro-4-[2-[N-methyl-N-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]amino]-1propoxy]benzoate as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-e3d5588593b24e22baef72e75de118d5
Source noteuspto-grants-2007_02