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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348489Generated: October 28, 2026

Ethyl bromoacetate → HCID 16005305, compound

https://huagongshe.com/reaction/348489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium CarbonateHCID 10340—
ReactantAcetonitrile--water (1/1)HCID 18373917—
ReactantHCID 178509063HCID 178509063—
SolventAcetoneHCID 180—
ProductHCID 16005305HCID 1600530576.3%

Reaction Steps

A solution of ethyl bromoacetate (0.128 g, 0.76 mmol) in acetone (2 mL) was added to a suspension of 4-amino-2-mercaptopyrimidine-5-carboxylic acid (4-fluorophenyl)amide (0.10 g, 0.38 mmol) and Na2CO3 (80 mg, 0.76 mmol) in acetone (5 mL). After stirring at ambient temperature for 2 hours, the resulting suspension was filtered and the filtrate concentrated to afford a crude solid that was recrystallized in dichloromethane/hexanes, or alternatively CH3CN/H2O) to afford the titled compound as a white solid (100 mg, 0.29 mmol, 76% yield). 1H NMR (300 MHz, d6-acetone) δ 9.60 (bs, 1H), 8.67 (s, 1H), 7.75 (m, 1H), 7.56 (m, 2H), 4.15 (m, 2H), 3.92 (s, 1H), 1.22 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176310B1
Source datasetuspto-grants-2007_02
ORD IDord-5812c06673994dbd82c24b91bb8f34fb
Source noteuspto-grants-2007_02