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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604369Generated: October 27, 2026

Sodium Acetate → HCID 11535765, compound

https://huagongshe.com/reaction/604369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant(2-Aminophenyl)boronic acidHCID 2773216—
ReactantMethyl 2-bromothiophene-3-carboxylateHCID 53302196—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductHCID 11535765HCID 1153576512%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a microwave vessel, methyl 2-bromo-3-thiophene carboxylate (1.0 eq, 64 mg, 0.29 mmol), 2-amino phenyl boronic acid (1.2 eq, 48 mg, 0.35 mmol), sodium acetate (3.0 eq, 71 mg, 0.86 mmol) and PdCl2(dppf) (0.1 eq, 15 mg, 0.028 mmol) were mixed together in anhydrous DMF (0.2 ml). The mixture was heated in a microwave oven at 120° C. for 5 nm. The material was purified by preparative HPLC. Acetonitrile was evaporated, and the compound was extracted with CH2Cl2 (3×). The combined extracts were washed with water, dried over Na2SO4, and the solvents removed in vacuo. Recrystallization in EtOH provided thieno[3,2-c]quinolin-4(5H)-one as a tan crystalline solid (7 mg, 12% yield). LCMS (ES): 95% pure, m/z 202 [M+1]+; 1H NMR (CDCl3/CD3OD, 9:1, 400 MHz) δ 7.28 (m, 1H), 7.33 (m, 1H), 7.43-7.50 (m, 2H), 7.74 (d, J=4.4, 1H), 7.82 (d, J=7.6, 1H) ppm

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910600B2
Source datasetuspto-grants-2011_03
ORD IDord-1bc109be9931464280e4f35a9dcd0aa9
Source noteuspto-grants-2011_03