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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193278Generated: November 2, 2026

3,4-Dimethylpentanoic acid → (3R)-Methyl 3-(3,4-dimethylpentanamido)-2,3-dihydro-1H-indene-5-carboxylate

https://huagongshe.com/reaction/1193278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethylpentanoic acidHCID 226113—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(R)-methyl 3-amino-2,3-dihydro-1H-indene-5-carboxylate hydrochlorideHCID 66700566—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(3R)-Methyl 3-(3,4-dimethylpentanamido)-2,3-dihydro-1H-indene-5-carboxylateHCID 6680531487%

Reaction Steps

HATU (0.872 g, 2.3 mmol, 1 eq) and TEA (0.647 ml, 4.6 mmol, 2 eq) were added to an ice-cooled solution of 3,4-dimethylpentanoic acid (300 mg, 2.3 mmol, 1 eq) in THF (26 ml), and stirring was carried out for 15 min. (3R)-3-Amino-2,3-dihydro-1H-indene-5-carboxylic acid methyl ester hydrochloride (A-01) (0.786 g, 3.5 mmol, 1.5 eq) was added to the reaction solution, and the mixture was then stirred overnight at RT. The reaction solution was diluted with ethyl acetate, washed with sat. sodium hydrogen carbonate solution and sat. NaCl solution, dried over magnesium sulfate and concentrated under reduced pressure. After purification by column chromatography (silica gel, cyclohexane:ethyl acetate 2:1), the desired product was obtained. Yield: 87% (0.61 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-40794eebb6bb4d01b8a30847d6d471bb
Source noteuspto-grants-2014_03