HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585165Generated: October 30, 2026
Sulfuryl chloride → HCID 22339120, compound
https://huagongshe.com/reaction/585165
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 22339121 | HCID 22339121 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22339120 | HCID 22339120 | 104.1% |
Reaction Steps
Alternate Method: Sulfuryl chloride (135 mg, 80.2 μL, 1 mmol) was added at room temperature to a dichloromethane (10 mL) solution of 3-(5-chloro-2-methoxy-phenyl)-3-fluoro-1-methylsulfanylmethyl-6-trifluoromethyl-1,3-dihydro-indol-2-one (420 mg, 1 mmol) in a round-bottomed flask equipped with nitrogen inlet and magnetic stirrer. After stirring the reaction mixture at room temperature for 20 minutes, the crude solution was concentrated in vacuo to afford 3-(5-chloro-2-methoxy-phenyl)-1-chloromethyl-3-fluoro-6-trifluoromethyl-1,3-dihydro-indol-2-one (425 mg, 100% crude yield) as a light yellow solution. Step C: Phosphoric acid mono-[3-(5-chloro-2-methoxy-phenyl)-3-fluoro-2-oxo-6-trifluoromethyl-2,3-dihydro-indol-1-ylmethyl] ester, bis-[tris(hydroxymethyl)ammoniummethane] salt
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06930100B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-dfd5a1ac67ac43579321427fde17170d |
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| Source note | uspto-grants-2005_08 |
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