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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454101Generated: October 29, 2026

Triphenylphosphine → 7-(3-(Ethylsulphonyl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline

https://huagongshe.com/reaction/454101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant3-(Ethanesulfonyl)propan-1-olHCID 12943303—
Reactant7-hydroxy-6-methoxy-4-(2-methyl-1H-indol-5-yloxy)quinazolineHCID 135763108—
SolventDichloromethaneHCID 6344—
Product7-(3-(Ethylsulphonyl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazolineHCID 2203056855.2%

Reaction Steps

Diethyl azodicarboxylate (117 mg, 0.67 mmol) was added in portions to a solution of 7-hydroxy-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (120 mg, 0.37 mmol), (prepared as described in Example 49), and 3-(ethylsulphonyl)-1-propanol (74 mg, 0.48 mmol) in methylene chloride (3.5 ml) and triphenylphosphine (176 mg, 0.67 mmol). After stirring for 2 hours at ambient temperature, the residue was poured onto a column of silica and eluted with ethyl acetate/methylene chloride (1/1) followed by methylene chloride/methanol (97/3 followed by 95/5). After removal of the solvent under vacuum, the residue was triturated with ether, filtered and dried under vacuum to give 7-(3-(ethylsulphonyl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (93 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-4c91bd87dc084929b8cc975b4d987d61
Source noteuspto-grants-2013_07