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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186295Generated: October 27, 2026

Sodium Bicarbonate → HCID 178511961, compound

https://huagongshe.com/reaction/1186295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-(2-(pyrrolidin-1-yl)ethyl)-1H-indol-5-amineHCID 29923770—
ReactantMethyl thiophene-2-carbimidothioate hydroiodideHCID 66704664—
SolventEthanolHCID 702—
ProductHCID 178511961HCID 17851196144.8%

Reaction Steps

A solution of 3-(2-(pyrrolidin-1-yl)ethyl)-1H-indol-5-amine (0.59 g, 2.57 mmol) in dry ethanol (10 mL) was treated with methyl thiophene-2-carbimidothioate hydroiodide (1.467 g, 5.15 mmol) at room temperature and the resulting mixture was stirred overnight. The reaction was basified with saturated NaHCO3 solution (50 mL) and product was extracted into CH2Cl2 (2×25 mL). The combined organic layer was washed with brine (20 mL) and dried (Na2SO4). Solvent was evaporated and crude was purified by column chromatography (2 M NH3 in MeOH:CH2Cl2, 1:9) to obtain N-(3-(2-(pyrrolidin-1-yl)ethyl)-1H-indol-5-yl)thiophene-2-carboximidamide (0.39 g, 1.152 mmol, 44.8% yield) as a solid. 1H NMR (DMSO-d6) δ 10.59 (s, 1H), 7.70 (d, 1H, J=2.7 Hz), 7.58 (d, 1H, J=3.9 Hz), 7.26 (d, 1H, J=6.3 Hz), 7.10-7.08 (m, 2H), 6.92 (s, 1H), 6.62 (d, 1H, J=6.3 Hz), 6.23 (s, 2H), 2.80 (t, 2H, J=6.0 Hz), 2.65 (t, 2H, J=5.4 Hz), 2.52-2.48 (m, 4H, merged with DMSO peak), 1.68 (s, 4H); ESI-MS (m/z, %): 339 (MH+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673909B2
Source datasetuspto-grants-2014_03
ORD IDord-aed51d0ec0fb49e2b83026875ad4b95a
Source noteuspto-grants-2014_03