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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975433Generated: October 30, 2026

Triethylamine → Benzoic acid, 3-methoxy-4-[[1-methyl-5-[[(4,4,4-trifluoro-2-methylbutyl)amino]carbonyl]-1H-indol-3-yl]methyl]-, methyl ester, (R)-

https://huagongshe.com/reaction/1975433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantMethyl 4-(5-carboxy-1-methylindol-3-ylmethyl)-3-methoxybenzoateHCID 9998178—
ReactantHCID 12004108HCID 12004108—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 3-methoxy-4-[[1-methyl-5-[[(4,4,4-trifluoro-2-methylbutyl)amino]carbonyl]-1H-indol-3-yl]methyl]-, methyl ester, (R)-HCID 1005066155.1%

Reaction Steps

A mixture of (R)-2-methyl-4,4,4-trifluorobutylamine hydrochloride (9.79 g), methyl 4-(5-carboxy-1-methylindol-3-ylmethyl)-3-methoxybenzoate (20.55 g), 4-dimethylaminopyridine (7.45 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (15.07 g) and triethylamine (9.3 mL) was dissolved in dry methylene chloride (240 mL) and the solution was stirred under an inert atmosphere for 18 h. The mixture was diluted with methylene chloride (200 mL) and washed twice with 1N hydrochloric acid. The combined acid washes were back extracted with methylene chloride and the combined organic extracts were washed (water, brine), dried (MgSO4), and evaporated. The residue was purified by flash chromatography, eluting with 97:3 methylene chloride:ethyl acetate to give methyl (R)-3-methoxy-4-[1-methyl-5-(2-methyl-4,4,4-trifluorobutylcarbamoyl)indol-3-ylmethyl]benzoate (14.48 g, 55%) as a white solid; mp 150°-151° C.; partial NMR (300 MHz, CDCl3): 1.12 (d, 3H, CH3), 1.98-2.08 (m, 1H, CHCH3) 2.12-2.44 (m, 2H, CF3CH2), 3.30-3.58 (m, 2H, CH2N), 3.76 (s, 3H, NCH3), 3.90 (s, 3H, OCH3), 3.93 (s, 3H, OCH3), 4.13 (s, 2H, ARCH2Ar'), 6.23 (br t, 1H, NHCO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286740
Source datasetuspto-grants-1994_02
ORD IDord-c140cbb13a214dca8be74befbfca1bcf
Source noteuspto-grants-1994_02