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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33732Generated: October 26, 2026

Sodium hydride → 1-(3-{4-[1-(3-Piperidin-1-yl-propyl)-1H-pyrrol-2-yl]-phenoxy}-propyl)-piperidine

https://huagongshe.com/reaction/33732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPiperidine, 1-(3-chloropropyl)-HCID 79625—
Reactant1-{3-[4-(1H-Pyrrol-2-yl)-phenoxy]-propyl}-piperidineHCID 17962613—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(3-{4-[1-(3-Piperidin-1-yl-propyl)-1H-pyrrol-2-yl]-phenoxy}-propyl)-piperidineHCID 1029497789.2%

Reaction Steps

To a stirred suspension of sodium hydride (0.051 g) in DMF (3 mL) at RT was added dropwise the product of Example 18 (0.2 g) in DMF (4 mL). After 20 min, 1-(3-chloro-propyl)-piperdine (0.139 g) was added dropwise and the mixture stirred for 12 h. The mixture was diluted with water and extracted several times with diethyl ether. The combined organic layers were washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure, giving the title compound as a dark red oil (0.257 g). 1H NMR (400 MHz, C6D6): 7.35 (d, J=8.8 Hz, 2H), 6.90 (d, J=8.8 Hz, 2H), 6.72 (t, J=2.5 Hz, 1H), 6.44 (d, J=2.5 Hz), 3.82 (m, 4H), 2.37-2.16 (m, 8H), 2.06 (br s, 4H), 1.96 (t, J=6.6 Hz, 2H), 1.87-1.81 (m, 2H), 1.59-1.22 (m, 16H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429586B2
Source datasetuspto-grants-2008_09
ORD IDord-cc46cb2230db48b88db4dd9f640a6651
Source noteuspto-grants-2008_09