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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893387Generated: October 30, 2026

Thionyl Chloride → HCID 68023578, compound

https://huagongshe.com/reaction/1893387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant5-Nitroindole-2-carboxylic acidHCID 351291—
ReactantSodium BicarbonateHCID 516892—
ReactantCalcium ChlorideHCID 5284359—
Solvent1,4-DioxaneHCID 31275—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 68023578HCID 68023578—

Reaction Conditions

Temperature25 °C

Reaction Steps

Thionyl chloride (8 ml, 110 mmol, 5 eq.) was added to a suspension of the compound of formula (III) (4.53 g, 22 mmol, 1 eq.) in dry dioxane (50 ml). The final suspension was refluxed in dry atmosphere (CaCl2 valve) for 2 h, and the reaction turned to a light brown solution while proceeding. The reaction was cooled to 25° C. and organic volatiles were removed under reduced pressure, then dry toluene (25 ml) was added and removed under vacuum, this operation was repeated twice. The brown residue (22 mmol, 1 eq.) was added portion wise to a cooled solution at 0° C. of NaHCO3 (3.7 g, 43.95 mmol, 2 eq.) and 2,2-dimethoxy-ethylamine (2.39 ml, 21.97 mmol, 1 eq.) in dioxane/water 4:1 (100 ml), the suspension was stirred for 2 hours at rt. Organic volatiles were removed under reduced pressure and the yellow precipitate was filtered and dried to give 5-nitro-1H-indole-2-carboxylic acid (2,2-dimethoxy-ethyl)-amide (IV). Yield=5.80 g (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513241B2
Source datasetuspto-grants-2013_08
ORD IDord-bbdd51e8671c429ab33699d0d610abab
Source noteuspto-grants-2013_08