HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178120Generated: October 30, 2026
Ammonium Chloride → HCID 117653151, compound
https://huagongshe.com/reaction/2178120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 3-Cyano-4-fluorobenzenesulfonyl chloride | HCID 2778908 | — |
| Reactant | HCID 63362875 | HCID 63362875 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117653151 | HCID 117653151 | 36% |
Reaction Steps
To a suspension of N-(2,4-dimethoxybenzyl)pyridazin-3-amine (Preparation 19, 1.0 g, 4.00 mmol) in THF (15 mL) at −20° C. was slowly added LiHMDS (1M, 4.0 mL, 4.00 mmol). The reaction mixture was left to stir at −20° C. for 30 minutes and then cooled to −78° C. To the reaction mixture was slowly added 3-cyano-4-fluorobenzene-1-sulfonyl chloride (0.8 g, 3.64 mmol) suspended in THF (15 mL). The reaction mixture was slowly warmed to room temperature and left at room temperature for 18 hours. To the vessel was added saturated aqueous NH4Cl solution (30 mL) and the product was extracted with EtOAc (25 mL). The organic layer was washed with saturated brine (40 mL), dried over MgSO4, and the solvent removed under vacuum. The residue was purified using silica gel column chromatography eluting with 70% EtOAc in heptanes to afford the title compound as an orange oil (561 mg, 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067922B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-ff9016a948c945e49b01aeddd44a0276 |
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| Source note | uspto-grants-2015_06 |
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