HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631Generated: October 25, 2026
2-Naphthalenesulfonic acid → HCID 19691974, compound
https://huagongshe.com/reaction/1631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenesulfonic acid | HCID 8420 | — |
| Reactant | 4,5-Dihydro-2-(methylthio)thiazole | HCID 88324 | — |
| Reactant | 4-Chloro-2,3-dihydro-1H-isoindole | HCID 14795868 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19691974 | HCID 19691974 | — |
Reaction Steps
A mixture of 4-chloroisoindoline (700 mg), 2-methylthio-2-thiazoline (600 mg), and β-naphthylsulfonic acid (35 mg) was heated at 150° C. for 30 minutes. The product was cooled, dissolved in methylene chloride, washed with water, the organic layer dried over anhydrous potassium carbonate, filtered, and solvent removed from the filtrate under reduced pressure. The residue was chromatographed on silica gel packed in methylene chloride/2% methanol/ammonia, eluting with methylene chloride/2% methanol, to give 4-chloro-2-(thiazolin-2-yl)isoindoline, a compound of Formula (IA), m.p. 167°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05726197 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-0591013fd92545f5bf5092992c26919f |
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| Source note | uspto-grants-1998_03 |
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