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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408602Generated: November 3, 2026

Sodium hydride → HCID 71268830, compound

https://huagongshe.com/reaction/2408602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Oxiran-2-yl)pyridineHCID 10953483—
ReactantHCID 71268754HCID 71268754—
SolventDimethylformamideHCID 6228—
ProductHCID 71268830HCID 712688304.9%

Reaction Steps

To a stirred solution of 1-(2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indol-8-yl)ethanone (80 mg, 0.35 mmol) in DMF (2 mL) was added sodium hydride (60%, 42 mg, 1.05 mmol). After stirring for 10 min, a solution of 4-(oxiran-2-yl)pyridine (62 mg, 0.51 mmol) in DMF (1 mL) was added into the reaction mixture, and stirred at RT for 4 h. The reaction mixture was quenched with ice water and extracted with EtOAc. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue obtain was purified by crystallization with ether to yield 1-(2,3,4,5-tetrahydro-5-(2-hydroxy-2-(pyridin-4-yl)ethyl)-2-methyl-1H-pyrido[4,3-b]indol-8-yl)ethanone (6 mg). 1H NMR (CDCl3, freebase) δ (ppm): 8.5 (d, 2H), 7.95 (s, 1H), 7.73 (d, 1H), 7.26 (d, 2H), 7.12 (d, 1H), 4.78 (t, 1H), 4.8 (d, 2H), 3.49 (m, 2H), 2.90 (m, 1H), 2.8 (q, 2H), 2.79 (s, 3H), 2.6 (m, 1H), 2.37 (s, 3H). Separation by chiral HPLC provided enantiomers 49a and 49b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815843B2
Source datasetuspto-grants-2014_08
ORD IDord-36ac1369a11c49ab92fa035a1f61946b
Source noteuspto-grants-2014_08