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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441265Generated: November 1, 2026

(Chlorothio)formyl chloride → HCID 68541084, compound

https://huagongshe.com/reaction/1441265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Chlorothio)formyl chlorideHCID 75990—
ReactantHCID 68538635HCID 68538635—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68541084HCID 6854108455.6%

Reaction Steps

To a suspension of 7-chloro-1-(tetrahydropyran-4-yl)methyl-1H-indole-3-carboxylic acid amide (8.0 g, 27.0 mmol) in tetrahydrofuran (100 ml) was added chlorocarbonylsulfenyl chloride (4.7 ml, 55.0 mmol) and the reaction mixture was heated at reflux for 3 h and allowed to cool. The precipitate was filtered off and dried to give 7-chloro-3-([1,3,4]-oxathiazol-2-on-5-yl)-1-(tetrahydropyran-4-yl)methyl-1H-indole (5.3 g, 15.0 mmol) as a white solid. The filtrate was concentrated in vacuo, and the resulting solid was washed with 5% ethyl acetate in n-heptane then dried to afford a further batch of 7-chloro-3-([1,3,4]-oxathiazol-2-on-5-yl)-1-(tetrahydropyran-4-yl)methyl-1H-indole (2.6 g, 7.0 mmol) as a pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655645B2
Source datasetuspto-grants-2010_02
ORD IDord-8a5614d03f694028af7b8b16c233c155
Source noteuspto-grants-2010_02