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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636820Generated: November 1, 2026

Phosphorus oxychloride → 4-Chloro-2-methyl-10-(2,4,6-trimethylphenyl)pyrido[2,3-b]indolizine

https://huagongshe.com/reaction/636820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178424432HCID 178424432—
Product4-Chloro-2-methyl-10-(2,4,6-trimethylphenyl)pyrido[2,3-b]indolizineHCID 1551327394%

Reaction Steps

A solution of 4-hydroxy-2-methyl-10-(2,4,6-trimethylphenyl)pyrido-[2,3-b]indolizine (10.1 g; 32 mmol) in phosphorus oxychloride (60 mL) is heated at 100° C. for 1 hour, cooled to room temperature, and concentrated in vacuo. The residue is partitioned into ice water and dichloromethane. The aqueous phase is separated and extracted twice with dichloromethane. The combined organics are washed with a 1 N aqueous sodium hydroxide solution and then with water. The solution is dried (Na2SO4), filtered, and concentrated in vacuo, and the resulting dark residue is filtered through a short pad of silica gel and washed with 25% ethyl acetate in hexane. The filtrate is concentrated in vacuo to give 10.1 g of the title compound as a yellow solid (94%): 1H nmr (400 MHz, CDCl3) d 2.00 (s, 6 H), 2.37 (s, 3 H), 2.64 (s, 3 H), 6.58 (t, 1 H), 6.95 (dd, 1 H), 7.00 (s, 2 H), 7.07 (s, 1 H), 7.08 (d, 1 H), 9.26 (d, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194574B1
Source datasetuspto-grants-2001_02
ORD IDord-261bcda3b81d4731a71b1e64047cbe6b
Source noteuspto-grants-2001_02