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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362888Generated: October 30, 2026

2-(Methylsulfonyl)ethanamine → HCID 57974158, compound

https://huagongshe.com/reaction/1362888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylsulfonyl)ethanamineHCID 4340561—
ReactantHCID 57974221HCID 57974221—
SolventDichloromethaneHCID 6344—
ProductHCID 57974158HCID 5797415820%

Reaction Steps

2-({5-Fluoro-2-[(4-formylphenyl)amino]-4-pyrimidinyl}amino)-N-(1-methylethyl)benzamide (80 mg, 0.2 mmol, 1.0 eq), [2-(methylsulfonyl)ethyl]amine (100 mg, 0.6 mmol, 3.0 eq), and CH2Cl2 (2.0 mL) were added to a vessel, which was sealed and stirred at room temperature for 16 h. Solvent was removed by evaporation to leave a residue. NaBCNH4 (37 mg, 0.6 mmol, 3.0 eq) in CH2Cl2 (2.0 mL) was added was added to the residue and the reaction mixture was stirred at room temperature until the reaction was substantially complete, as determined by HPLC. The final product was purified by preparative HPLC using water (0.1% formic acid); acetonitrile (0.1% formic acid) as mobile phase. The desired compound was isolated as an off-white solid. (20 mg, 20% yield) MS: M(C24H29FN6O3S)=500.60, (M+H)+=501.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884098B2
Source datasetuspto-grants-2011_02
ORD IDord-8ed396cd039b4823a5307b312230175f
Source noteuspto-grants-2011_02