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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882164Generated: October 31, 2026

Ethylenediamine → HCID 89630021, compound

https://huagongshe.com/reaction/882164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 89615759HCID 89615759—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 89630021HCID 89630021—

Reaction Conditions

Temperature50 °C

Reaction Steps

To N-(3-(5-(oxazol-2-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)methacrylamide (140 mg, 0.295 mmol) was added portionwise, a solution of trifluoroacetic acid (3.4 g, 30 mmol) in dichloromethane (10 mL). The reaction was stirred for 1 hour at 50° C., then concentrated in vacuo. To this crude reaction mixture was added ethane-1,2-diamine (35 mg, 0.59 mmol), followed by portionwise addition of a solution of sodium hydroxide (82 mg, 2.1 mmol) in methanol (10 mL). After stirring at room temperature for 30 minutes, the reaction mixture was concentrated in vacuo and extracted with ethyl acetate (×3). The combined organic layers were washed with brine, dried with anhydrous sodium sulfate, filtered and concentrated in vacuo. Purification of the crude product by reverse phase HPLC using an acetonitrile gradient in water with 0.5% TFA modifier afforded N-(3-(5-(oxazol-2-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)methacrylamide as a green solid. LRMS (ESI) calc'd for C19H16N5O2 [M+H]+: 346, found 346. 1H NMR (400 MHz, CD3OD) δ 9.05 (s, 1H), 8.25 (s, 1H), 7.93 (s, 1H), 7.80 (d, 1H, J=8.0 Hz), 7.59 (s, 1H), 7.38-7.42 (m, 1H), 7.26 (d, J=8.0 Hz, 1H), 7.13 (s, 1H), 5.80 (s, 1H), 5.55 (s, 1H), 1.99 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993756B2
Source datasetuspto-grants-2015_03
ORD IDord-68a1f799466c4106af17395fb32fe59d
Source noteuspto-grants-2015_03