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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902837Generated: October 29, 2026

Diisopropylethylamine → N-[(1R*,2S*)-2-Aminocyclopropyl]-5-chloroindole-2-carboxamide

https://huagongshe.com/reaction/902837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-1H-indole-2-carboxylic acidHCID 82693—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactantcis-1,2-Cyclopropanediamine hydrochlorideHCID 66785209—
SolventDimethylformamideHCID 6228—
ProductN-[(1R*,2S*)-2-Aminocyclopropyl]-5-chloroindole-2-carboxamideHCID 18442851—

Reaction Steps

1-Hydroxybenzotriazole monohydrate (377 mg), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (642 mg) and diisopropylethylamine (1.95 ml) were added to a solution of cis-1,2-cyclopropanediamine hydrochloride (J. Med. Chem., 1998, Vol. 41, pp. 4723-4732) (405 mg) and 5-chloroindole-2-carboxylic acid (546 mg) in N,N-dimethylformamide (10 ml) at room temperature, and the mixture was stirred for 50 hours. After the reaction mixture was concentrated under reduced pressure, methylene chloride (50 ml) and a saturated solution (200 ml) of sodium hydrogencarbonate were added to separate colorless solid deposited by filtration. The filtrate was extracted with methylene chloride. After the resultant organic layers were combined and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure to obtain residue. The residue was purified by flash column chromatography on silica gel (methylene chloride:methanol=100:7→10:1) to obtain the title compound (110 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365205B2
Source datasetuspto-grants-2008_04
ORD IDord-db882049ef5a4426806c66f36c94383d
Source noteuspto-grants-2008_04