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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069017Generated: October 30, 2026

4-Methylmorpholine → HCID 10140471, compound

https://huagongshe.com/reaction/1069017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
ReactantHCID 21190753HCID 21190753—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10140471HCID 1014047119.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2.7 grams of disulfide acid from Example 74 in 25 mL of tetrahydrofuran was cooled in an ice bath. A 1.9 mL portion of isobutylchloroformate followed by a 1.6 mL portion of N-methyl morpholine were added. After stirring for 5 minutes at 0° C., 1.0 grams of N-(3-bromophenyl)4,6-quinazolindiamine was added. The mixture was stirred for 3 hours at 0° C. and then allowed to warm to room temperature. The reaction was quenched with water and the tetrahydrofuran was evaporated under vacuum. Addition of methylene chloride followed by washing the methylene chloride layer with water and evaporation of the solvent gave a crude product. Silica gel chromatography with methanol in methylene chloride gave 0.3 grams white solid of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-32ea2aa22d82444da7ab0efa3ee4fbe4
Source noteuspto-grants-2001_06