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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014427Generated: November 1, 2026

Hydrochloric Acid → HCID 67316367, compound

https://huagongshe.com/reaction/1014427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(3-Amino-4-methylphenyl)-N~2~,N~2~-dimethylglycinamideHCID 17607975—
ReactantHCID 25150094HCID 25150094—
SolventDichloromethaneHCID 6344—
ProductHCID 67316367HCID 67316367823.8%

Reaction Steps

To a pressurized vessel was added 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamide (1.0 g, 2.27 mmol), N1-(3-amino-4-methylphenyl)-N2,N2-dimethylglycinamide (0.590 g, 2.83 mmol), potassium iodide (<10 mg) and hydrochloric acid as a 4.0M solution in dioxanes (ca 4 mL). The resulting suspension was stirred until all solids had completely dissolved (24 hr.) The reaction was poured into into saturated sodium bicarbonate and diluted with dichloromethane. The organic layer was dried over sodium sulfate, volatiles removed under reduced pressure, and the solids triturated with diethyl ether to afford N2,N2-dimethyl-N1-[4-methyl-3-({3-[(4-methylphenyl)sulfonyl]-7-oxo-3,7-dihydropyrrolo[2′,3′:4,5]pyrimido[6,1-b]quinazolin-5-yl}amino)phenyl]glycinamide (1.11 g, 18.7 mmol, 82% yield) of sufficient purity for use in subsequent transformations. ESIMS (M+H)=596.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-d54ebd19625045e58ed574fbbbb7f8e3
Source noteuspto-grants-2011_07