HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362888Generated: October 30, 2026
2-(Methylsulfonyl)ethanamine → HCID 57974158, compound
https://huagongshe.com/reaction/1362888
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Methylsulfonyl)ethanamine | HCID 4340561 | — |
| Reactant | HCID 57974221 | HCID 57974221 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57974158 | HCID 57974158 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884098B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-8ed396cd039b4823a5307b312230175f |
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| Source note | uspto-grants-2011_02 |
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