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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803428Generated: November 1, 2026

1,2-Dichloroethane → HCID 59580759, compound

https://huagongshe.com/reaction/1803428

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
ReactantHCID 59580893HCID 59580893—
SolventAcetic AcidHCID 176—
ProductHCID 59580759HCID 5958075945%

Reaction Conditions

Temperature65 °C

Reaction Steps

To N-[2-(5-fluoro-pyridin-3-yl)-thiazol-5-yl]-N-methyl-3-methylsulfanyl-propionamide (Compound 30, 44 mg, 0.14 mmol) in glacial acetic acid (1.5 mL) was added sodium perborate tetrahydrate (23 mg, 0.14 mmol), and the mixture was heated at 65° C. for 2 h. The reaction mixture was carefully poured into a separatory funnel containing saturated aqueous NaHCO3 resulting in gas evolution. When the gas evolution had ceased, DCE was added and the layers were separated. The aqueous layer was extracted twice with DCE, and all the organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure to give the desired product as white solid (20 mg, 45%): mp 152-154° C.; 1H NMR (300 MHz, CDCl3) δ 8.95 (s, 1H), 8.59 (s, 0.3H), 8.49 (s, 0.7H), 7.98 (d, J=9.3 Hz, 1H), 7.73 (s, 0.3H), 7.62 (s, 0.7H), 3.64 (s, 2.1H), 3.36 (s, 0.9H), 3.40-2.70 (m, 4H), 2.69 (s, 2.1H), 2.61 (s, 0.9H); ESIMS m/z 328.1 (M+1), m/z 326.1 (M-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350044B2
Source datasetuspto-grants-2013_01
ORD IDord-e8f070551438489a8be44cd1d0ff59dd
Source noteuspto-grants-2013_01