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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825718Generated: November 3, 2026

Hydrochloric Acid → HCID 9859833, compound

https://huagongshe.com/reaction/1825718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylamineHCID 674—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22139459HCID 22139459—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 9859833HCID 9859833100%

Reaction Steps

3-(3-oxocyclopentyl)-1H-indole-5-carbonitrile (2.24 g, 10 mMol) and dimethylamine (2.0 M solution in THF, 50 mL, 100 mMol) were dissolved in EtOH (150 mL). After stirring for 15 min, sodium triacetoxyborohydride (8.50 g, 40 mMol) was added and the reaction stirred for 4 h. The reaction was then diluted with water (100 mL) and made acidic (pH 3) with HCl (6 M). The reaction was then adjusted to pH 10 with sodium carbonate. It was extracted three times with ethyl acetate (100 mL) and the organic extracts were dried over sodium sulfate, concentrated in vacuo, and dried under high vacuum to give 3-(3-dimethylaminocyclopentyl)-1H-indole-5-carbonitrile (Compound 3, 2.5 g, 100%) as mixture of cis/trans diastereomers. 1H NMR (500 MHz, d4-MeOH) δ 8.02 (0.7 H s), 7.99 (0.3 H, s), 7.46 (0.4 H, s), 7.44 (0.6 H, s), 7.35 (1 H, dd, J=8.55 1.53), 7.24 (0.7 H, s), 7.21 (0.3 H, s), 3.49 (0.4 H, m), 3.37 (0.6 H, m), 2.92 (0.3 H, m), 2.83 (0.7 H, m), 2.41 (0.7 H, m), 2.36 (6 H, s), 2.22 (1.3 H, m), 2.07 (1 H, m), 1.80 (2 H, m), 1.67 (1 H, m). MS m/e 254.2 (M+H)+, 252.2 (M−H)+. LCMS (YMC ODS-A C18 S7 3.0×50 mm) tR, 0.857 min., MH+ 254.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049314B2
Source datasetuspto-grants-2006_05
ORD IDord-8af91ecf23c34be0a689dc47cd1c459a
Source noteuspto-grants-2006_05