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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966473Generated: October 29, 2026

Water → HCID 23393870, compound

https://huagongshe.com/reaction/966473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23393871HCID 23393871—
SolventDimethylformamideHCID 6228—
ProductHCID 23393870HCID 2339387069.1%

Reaction Steps

To a suspension of NaH (0.959 mmol, 0.038 g, 60% in mineral oil, rinsed twice with hexanes) in 5 mL of DMF at 0° C. under N2 was added a solution of 5-(2-chloro-ethoxy)-2-methyl-1H-indole-3-carboxylic acid benzyl ester (0.873 mmol, 0.300 g, Example 1, Step A) in 3.73 mL of DMF. The ice bath was removed and the solution was stirred for 2 hours at room temperature. Methyl iodide (0.959 mmol, 0.060 mL, Aldrich) was added dropwise via syringe and the solution was stirred for 20 hours. Water (10 mL) was added and the mixture was stirred for 30 minutes. The resulting precipitate was filtered off, the filtrate was extracted with ether (3×10 mL), and the extracts were washed with water (2×10 mL), brine (1×10 mL), dried over MgSO4, and concentrated. The residue was combined with the solid and purified by silica gel flash column chromatography (30% ethyl acetate/hexanes) to give a white solid (0.216 g, 69%): 1HNMR (400 MHz, DMSO-d6) δ 2.67 (s, 3H, ArCH3), 3.66 (s, 3H, NCH3), 3.87-3.89 (m, 2H, CH2Cl), 4.09-4.12 (m, 2H, CH2OAr), 5.29 (s, 2H, CO2CH2Ph), 6.80-6.83 (m, 1H, ArH), 7.21-7.50 (m, 7H, ArH); MS(APCI+): m/z 358.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951848B2
Source datasetuspto-grants-2005_10
ORD IDord-d51f1e63702540deb71eab25ac67b867
Source noteuspto-grants-2005_10