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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425002Generated: October 28, 2026

Hydrochloric Acid → HCID 44603793, compound

https://huagongshe.com/reaction/2425002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 67245854HCID 67245854—
SolventEthanolHCID 702—
ProductHCID 44603793HCID 4460379311.2%

Reaction Steps

1-(3′-Acetamido-4′-methoxybenzenesulfonyl)-5-methoxy-3-methyl-1H-indole (10 grams, 25.7 mmol) (obtained from preparation 1) was taken into a 250 mL of three necked round bottom flask containing ethanol (100 mL) and stirred the mass to obtain a clear solution. Aqueous hydrochloric acid (10 mL, 33%) was added to this clear solution and heated the mass at reflux temperature for a period of two hours. The progress of the reaction was monitored by thin layer chromatography. After completion of the reaction, the reaction mass was concentrated under vacuum and the residual mass was quenched into chilled water (100 mL). The pH was adjusted to 9.0 to 10.0 with dilute sodium hydroxide solution. The product was extracted with dichloro methane (2×100 mL). Organic phase was washed with brine solution, dried over anhydrous sodium sulphate and concentrated the mass under reduced pressure to obtain crude compound. The obtained technical product was purified by column chromatography using silica gel (100-200 mesh), the eluent system being ethyl acetate and n-hexane (2:8) to obtain 1.0 gram of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964627B2
Source datasetuspto-grants-2011_06
ORD IDord-41d709908fe94ee4b77ba386574b1bc9
Source noteuspto-grants-2011_06