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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177543Generated: November 1, 2026

Dimethylformamide → HCID 67111889, compound

https://huagongshe.com/reaction/1177543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 67111838HCID 67111838—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 67111889HCID 67111889—

Reaction Conditions

Temperature80 °C

Reaction Steps

In a sealable bottle, sodium tert-butoxide (0.120 g, 1.25 mmol) was added to a mixture of acetamidomalonic acid diethyl ester (0.272 g, 1.25 mmol) in THF (10.00 ml)/DMF (2.00 ml). The reaction was heated to 80° C. for 20 min., cooled to ambient temperature, and a solution of 2-(4-(bromomethyl)-2-fluorophenyl)-5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine (0.500 g, 1.14 mmol) in THF 4 ml was added slowly dropwise. The resulting mixture was heated to reflux (90 deg. C.) for 1.5 h, and the color changed from orange to yellow. The reaction was cooled, poured over ice water, and treated with EtOAc. The organic layer was washed with water, NaCl, dried over MgSO4, filtered, and concentrated in vacuo. Purification by silica gel chromatography, 40 g column, 10-30% EtOAc/hexanes, followed by 30-50% (3% Et3N in EtOAc)/hexanes provided diethyl 2-acetamido-2-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzyl)malonate. MS (ESI) m/z: calculated: 575.2; Observed: 576.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-e3b3cc11cfa5441abecc77b6fd283646
Source noteuspto-grants-2010_11