HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685082Generated: November 1, 2026
3-Fluorobenzyl isocyanate → HCID 58055089, compound
https://huagongshe.com/reaction/1685082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluorobenzyl isocyanate | HCID 643499 | — |
| Reactant | 3-(Chloromethyl)-1,2,4-thiadiazol-5-amine | HCID 14012604 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 58055089 | HCID 58055089 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148380B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-1b0d1ed5707f46eaa4a379af29dfcaf6 |
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| Source note | uspto-grants-2012_04 |
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