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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685082Generated: November 1, 2026

3-Fluorobenzyl isocyanate → HCID 58055089, compound

https://huagongshe.com/reaction/1685082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzyl isocyanateHCID 643499—
Reactant3-(Chloromethyl)-1,2,4-thiadiazol-5-amineHCID 14012604—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 58055089HCID 5805508972%

Reaction Steps

3-Fluorobenzyl isocyanate (1.3 g, 8 mmol) was added into a mixture of Intermediate 38: 3-chloromethyl-[1,2,4]thiadiazol-5-ylamine (0.83 g, 5.5 mmol), and DMAP (22 mg, 0.14 mmol) in NMP (11 mL). The reaction mixture was heated in a microwave reactor for 1 hour at 100 C and then cooled to ambient temperature. The reaction mixture was diluted with EtOAc (75 mL) and washed with water (30 mL×2). The aqueous phase was extracted with EtOAc (40 mL×2). The combined organic layers were washed with brine, dried over Na2SO4, filtered and evaporated to give the crude product, which was purified by silica gel column chromatography to afford 1-(3-chloromethyl-[1,2,4]thiadiazol-5-yl)-3-(3-fluoro-benzyl)-urea as an off-white solid (1.2 g, 72%). LC-MS (m/z): 303.0 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148380B2
Source datasetuspto-grants-2012_04
ORD IDord-1b0d1ed5707f46eaa4a379af29dfcaf6
Source noteuspto-grants-2012_04