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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773285Generated: November 1, 2026

Sodium hydride → HCID 49779379, compound

https://huagongshe.com/reaction/1773285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(2-Methyloxiran-2-yl)pyridineHCID 12395386—
Reactant1253640-41-3HCID 54588462—
SolventDimethylformamideHCID 6228—
ProductHCID 49779379HCID 49779379—

Reaction Steps

To a stirred solution of 6-methoxy-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (500 mg, 2.3 mmol) in DMF (10 mL) was added sodium hydride (276 mg, 6.9 mmol) and stirred for 10 min at RT, followed by addition of 4-(2-methyl-oxiranyl)-pyridine (468 mg, 3.4 mmol) and stirring continued for another 16 h. The reaction mixture was poured into ice water and extracted with EtOAc. The organic layer was washed with water, dried over sodium sulfate and concentrated to afford crude material, which was re-crystallized in ether and hexane to yield 1-(6-methoxy-2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)-2-(pyridin-4-yl)propan-2-ol. 1H NMR (CD3OD, TFA salt) d (ppm): 8.60 (m, 2H), 7.95 (m, 2H), 6.95 (m, 2H), 6.50 (m, 1H), 4.65 (m, 2H), 4.30 (m, 2H), 3.90 (m, 2H), 3.80 (s, 3H), 3.60 (m, 2H), 3.10 (s, 3H), 1.70 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255094B2
Source datasetuspto-grants-2016_02
ORD IDord-a494a505ab2049f8bcff63430739ba8e
Source noteuspto-grants-2016_02