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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23984Generated: October 30, 2026

Sodium Hydroxide → 2-({5-[3(2-Pyridylamino)propoxy]indolyl}methyl)octanoic acid

https://huagongshe.com/reaction/23984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-({5-[3-(2-pyridylamino)propoxy]indolyl}methyl)octanoateHCID 22570317—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-({5-[3(2-Pyridylamino)propoxy]indolyl}methyl)octanoic acidHCID 22570319891.9%

Reaction Steps

To a solution of methyl 2-({5-[3-(2-pyridylamino)propoxy]indolyl}methyl)octanoate (0.04 g, 0.09 mmol), as prepared in the preceding step, in methanol (5.0 mL) was added a solution of NaOH (0.1 g, 2.5 mmol) in H2O (0.3 mL), and the reaction was stirred at ambient temperature overnight. After evaporating the solvent in vacuo, the residue is taken up in H2O (5 mL) and acidified to pH 4-5 with 10% HCl, and extracted with ethyl acetate (2×15 mL). The combined organic layers were washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography on silica gel (4% methanol in methylene chloride) to give the title compound as an oil (0.34 g, 90%). 1H-NMR (400 MHz, CDCl3) δ 7.72 (m, 1H), 7.48 (m, 1H), 7.26 (d, 8.9 Hz, 1H), 7.02 (d, J=2.7 Hz, 2H), 6.77 (dd, J=8.9, 2.4 Hz, 1H), 6.50 (m, 2H), 6.28 (d, J=2.9 Hz, 1H), 4.27 (dd, J=14.2, 8.6 Hz, 1H), 3.99 (m, 3H), 3.32 (t, J=6.7 Hz, 2H), 2.85 (br s, 1H), 1.95 (m, 2H), 1.67 (m, 1H), 1.30 (m, 9H), 0.84 (t, J=6.6 Hz, 3H). Mass spectrum (LCMS, ESI pos.) Calcd. for C25H33N3O3 424.2 (M+H); Found: 424.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855722B2
Source datasetuspto-grants-2005_02
ORD IDord-13be62dcdae145d2a982a5d607870993
Source noteuspto-grants-2005_02