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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507488Generated: October 29, 2026

Triethylamine → HCID 5329096, compound

https://huagongshe.com/reaction/507488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 5329095HCID 5329095—
SolventDichloromethaneHCID 6344—
ProductHCID 5329096HCID 532909644%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a 0-5° C. stirred suspension of 2-[4-(3-bromo-phenylamino)-pyrido[3,4-d]pyrimidine-6-sulfonyl]-ethanol (41 mg, 0.1 mmol), and triethylamine (31 μL, 0.22 mmol) in dichloromethane (0.5 mL) under N2 was added dropwise methanesulfonyl chloride (9.3 μL, 0.12 mmol). Additional charges of methanesulfonyl chloride (9.3 μL, 9.3 μL) were added after 45 minutes, and 1.5 hours, the latter with additional triethylamine (50 μL). After reaction for a total of 2.5 hours, the cold solution was quenched with 5% aqueous sodium bicarbonate, then extracted with ethyl acetate (2×). The combined organic extracts were dried (MgSO4) then filtered through a pad of flash SiO2. The filtrate was concentrated to a solid that was crystallized from ethyl acetate to leave the product (17 mg, 44%), mp 214-217° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786131B2
Source datasetuspto-grants-2010_08
ORD IDord-1565c19de61f4b60b41860b933f17c20
Source noteuspto-grants-2010_08