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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020273Generated: November 3, 2026

Dichloromethane → HCID 69192623, compound

https://huagongshe.com/reaction/1020273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-MethoxyethanolHCID 8019—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58055089HCID 58055089—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69192623HCID 69192623—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (4 eq, 2.66 mmol, 0.13 g of a 50 wt-% suspension in oil) was suspended in THF (2 mL) and cooled to 0° C. 2-methoxy ethanol (3 eq, 1.99 mmol, 0.15 g) and 15-crown-5-ether (1 drop) were added. 1-(3-Fluorobenzyl)-3-(3-(chloromethyl)-1,2,4-thiadiazol-5-yl)urea (Intermediate XXV) was added and the mixture was stirred over night with temperature allowed to rise to room temperature. Dichloromethane (50 mL) was added. The mixture was washed with water (2×10 mL), dried (Na2SO4), filtered and concentrated in vacuo. The crude material (0.2 g of an oil) was further purified by preparative HPLC to give 0.101 g. 1H-NMR (300 MHz, CD3OD): δ 7.34 (m, 1H), 7.14 (d, 1H), 7.07 (d, 1H), 6.99 (m, 1H), 4.58 (s, 2H), 4.45 (s, 2H), 3.70 (t, 2H), 3.56 (t, 2H), 3.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716320B2
Source datasetuspto-grants-2014_05
ORD IDord-f5f8a67c92dd4b9f9370aa846e916fce
Source noteuspto-grants-2014_05