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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989383Generated: October 25, 2026

Sodium Iodide → 4-(2,4-Dichloro-5-methoxyphenylamino)-7-methoxy-8-(3-morpholinyl-propoxy)benzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/989383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMorpholineHCID 8083—
Reactant8-(3-Chloropropoxy)-4-(2,4-dichloro-5-methoxyphenylamino)-7-methoxybenzo[g]quinoline-3-carbonitrileHCID 10142598—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(2,4-Dichloro-5-methoxyphenylamino)-7-methoxy-8-(3-morpholinyl-propoxy)benzo[g]quinoline-3-carbonitrileHCID 10231532—

Reaction Steps

Following procedure 1 of Example 149, a mixture of 0.105 g (0.20 mmol) of 8-(3-chloropropoxy)-4-(2,4-dichloro-5-methoxyphenylamino)-7-methoxybenzo[g]quinoline-3-carbonitrile, 0.3 mL of morpholine and 0.01 g of sodium iodide in 10 mL of 1,2-dimethoxyethane is heated under reflux for 7 hours. The resulting solid is purified by silica gel chromatography, utilizing a 98:2 to 94:6 gradient of methylene chloride/methanol to give 0.089 g of 4-(2,4-dichloro-5-methoxyphenylamino)-7-methoxy-8-(3-morpholin-4-yl-propoxy)benzo[g]quinoline-3-carbonitrile as a yellow solid, mp 205-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638929B2
Source datasetuspto-grants-2003_10
ORD IDord-c84e156c4e4d4c6f8b956ca394f17a15
Source noteuspto-grants-2003_10