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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255975Generated: October 26, 2026

(Diethylamino)sulfur trifluoride → (4,5-Dichloro-2-fluoro-phenyl)-{7-[2-(2-fluoro-ethoxy)-ethoxy]-6-nitro-quinazolin-4-yl}-amine

https://huagongshe.com/reaction/1255975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
Reactant2-{2-[4-(4,5-Dichloro-2-fluoro-phenylamino)-6-nitro-quinazoline-7-yloxy]-ethoxy}-ethanolHCID 69266955—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(4,5-Dichloro-2-fluoro-phenyl)-{7-[2-(2-fluoro-ethoxy)-ethoxy]-6-nitro-quinazolin-4-yl}-amineHCID 8661884478.4%

Reaction Steps

DAST (0.16 gram, 1 mmol) was added slowly to a cooled solution (−78° C.) of Compound 29a (0.047 gram, 0.1 mmol) in dichloromethane (2 ml) and the resulting mixture was allowed to warm to room temperature and was thereafter stirred for 12 hours. The reaction mixture was then poured to a saturated solution of sodium bicarbonate), diluted with water, extracted thrice with dichloromethane, washed with brine, and dried over sodium sulfate. Removal of the solvent under reduced pressure afforded Compound 35a (0.036 gram, 78% yield) having a purity of 94%, as determined by HPLC. The compound was used in the following procedures without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461166B2
Source datasetuspto-grants-2013_06
ORD IDord-b373c4aeec224406a66f15adac73452b
Source noteuspto-grants-2013_06