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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630581Generated: October 31, 2026

Sodium hydride → HCID 68283646, compound

https://huagongshe.com/reaction/1630581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Oxiran-2-yl)pyridineHCID 10953483—
ReactantHCID 67312065HCID 67312065—
SolventDimethylformamideHCID 6228—
ProductHCID 68283646HCID 68283646—

Reaction Steps

To a solution of 2-allyl-2,3,4,5-tetrahydro-8-methyl-1H-pyrido[4,3-b]indole (1000 mg, 4.42 mmol) in DMF (10 mL) was portionwise added sodium hydride (526 mg, 13.26 mmol). After stirring at RT for 5 min., 4-(oxiran-2-yl)pyridine (669 mg, 5.31 mmol) was added dropwise into the reaction mixture, which was stirred at RT for 16 h. Ice water was added into the reaction mixture and the solid mass obtained was filtered, washed with water (2×10 mL), hexane (2×50 mL) and ether to yield 2-(2-allyl-1,2,3,4-tetrahydro-8-methylpyrido[4,3-b]indol-5-yl)-1-(pyridin-4-yl)ethanol. 1H NMR (CDCl3, freebase) δ (ppm): 8.6 (d, 2H), 7.24 (s, 1H), 7.2 (d, 2H), 7.0 (d, 2H), 5.98 (m, 1H), 5.2 (dd, 2H), 5.0 (m, 1H), 4.1 (m, 2H), 3.6 (dd, 2H), 3.22 (d, 2H), 2.7-2.9 (m, 3H), 2.6 (m, 1H), 2.4 (s, 3H). Separation by chiral HPLC provides enantiomers II-63a-b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791132B2
Source datasetuspto-grants-2014_07
ORD IDord-240951dd12174230a5c7178d0c3a7d68
Source noteuspto-grants-2014_07