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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785156Generated: November 1, 2026

Tetrahydrofuran → HCID 68881362, compound

https://huagongshe.com/reaction/1785156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant5-Chloro-7-(3-methoxyprop-1-ynyl)-1,3-benzodioxol-4-amineHCID 21082716—
Reactant4-Chloro-7-(2-chloroethoxy)-6-methoxyquinazolineHCID 59682907—
SolventDimethylformamideHCID 6228—
ProductHCID 68881362HCID 68881362—

Reaction Steps

A solution of sodium bis(trimethylsilyl)amide (5.6 ml) in tetrahydrofuran (1.0M, 5.6 mmol) was added dropwise to an ice-cold solution of 4-chloro-7-(2-chloroethoxy)-6-methoxyquinazoline (0.7 g, 2.6 mmol) and 5-chloro-7-(3-methoxyprop-1-yn-1-yl)-1,3-benzodioxol-4-amine (0.675 g, 2.8 mmol) in dimethylformamide (8 ml). The mixture was allowed to warm to room temperature over 3 hours. A saturated solution of ammonium chloride was added and the mixture was partitioned between water and dichloromethane. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure. Flash chromatography on silica eluting with a mixture of 30-100% ethyl acetate in hexane gave the product as a solid. (0.608 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504408B2
Source datasetuspto-grants-2009_03
ORD IDord-c68572d711c844ab8834df9b2d660fa7
Source noteuspto-grants-2009_03