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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992747Generated: October 31, 2026

3,4,5-Trimethoxybenzoic Acid → HCID 68681847, compound

https://huagongshe.com/reaction/1992747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-Trimethoxybenzoic AcidHCID 8357—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant(S)-2-(1-BOC-2-pyrrolidinyl)acetic acidHCID 688605—
ReactantHCID 79330684HCID 79330684—
Catalyst1-HydroxybenzotriazoleHCID 75771—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 68681847HCID 68681847—

Reaction Steps

Experimental condition analogous to Example 2 were used with 2-(S)-{[3-(2,4-difluoro-phenyl)-2-methyl-allylaminmo]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester were used with 2-(S)-carboxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester and 3-(2,4-difluoro-phenyl)-2-methyl-propenal described in scheme 15) 0.4 g (1 mmol), 3,4,5-trimethoxy benzoic acid 0.27 g (1.3 mmol), triethylamine 0.1 ml, 1-(dimethylaminopropyl)-3-ethylcarbodiimide 0.31 g (1.63 mmol), and 1-hydroxybenzotriazole 0.014 g (0.1 mmol) in 10 ml DCM. The reaction yielded 0.49 g of 2-(S)-{[3-(2,4-difluoro-phenyl)-2-methyl-allylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester. The compound was transformed to the HCl salt, yielding 45 mg of a white solid. Yield: 14%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649011B2
Source datasetuspto-grants-2010_01
ORD IDord-399dd36180dc4f5c9ed40799c6b13287
Source noteuspto-grants-2010_01