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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379150Generated: October 30, 2026

Water → 2,3,4,5-tetrahydro-5-methyl-2-[(4-methyloxazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one

https://huagongshe.com/reaction/2379150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant5-(Chloromethyl)-4-methyl-1,3-oxazoleHCID 205485—
Reactant1H-Pyrido(4,3-b)indol-1-one, 2,3,4,5-tetrahydro-5-methyl-HCID 11790213—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2,3,4,5-tetrahydro-5-methyl-2-[(4-methyloxazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-oneHCID 1895772613.6%

Reaction Steps

Sodium hydride (60% dispersion in oil; 600 mg) was added to a stirred suspension of 2,3,4,5-tetrahydro-5-methyl-1H-pyrido[4,3-b]indol-1-one (1.5 g) in dry DME (150 ml) and then the mixture was stirred at 60° for 5 h under nitrogen. 5-Chloromethyl-4-methyloxazole (1.2 g) was added and the mixture was stirred overnight. A further quantity of sodium hydride (60% dispersion in oil; 600 mg) was added and the mixture was stirred at 60° for 4 h, then cautiously treated with water (100 ml). The mixture was extracted with dichloromethane containing methanol (ca. 1%) (3×100 ml) and the combined extracts were evaporated. The residue was purified by FCC eluting with System A (100:8:1) to give the title compound (300 mg) as a solid, t.l.c. (System A, 100:8:1) Rf 0.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05360800
Source datasetuspto-grants-1994_11
ORD IDord-78ab3621225e4826aede54a4a4ab6b59
Source noteuspto-grants-1994_11