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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50122Generated: October 27, 2026

Diisopropylethylamine → n-((Dimethylamino)acetyl)-1-methyl-n-(3,4,5-trimethoxyphenyl)-1h-indole-5-sulfonamide

https://huagongshe.com/reaction/50122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-methyl-N-(3,4,5-trimethoxyphenyl)-1H-indole-5-sulfonamideHCID 9929571—
Reactant2-(Dimethylamino)acetyl chloride hydrochlorideHCID 13994991—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Productn-((Dimethylamino)acetyl)-1-methyl-n-(3,4,5-trimethoxyphenyl)-1h-indole-5-sulfonamideHCID 995595092%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of Example 4 (20.0 g, 53.2 mmol) in THF (250 mL) at room temperature was treated with dimethylaminoacetyl chloride hydrochloride (12.3 g, 77.8 mmol), DMAP (650 mg, 5.3 mmol), and diisopropylethylamine (25.2 g, 195.0 mmol), stirred for 8 hours, and concentrated to ⅓ its original volume. The mixture was diluted with ethyl acetate (400 mL), washed with 5% NaHCO3 (2×200 mL) and water (200 mL), dried (Na2SO4), filtered, concentrated to a volume of 120 mL, diluted with methyl tert-butyl ether (120 mL), stirred for 18 hours, cooled to 0° C., stirred for 2 hours, and filtered. The resulting solid was washed with 1:1 ethyl acetate/methyl tert-butyl ether (100 mL) and dried under vacuum to provide 22.5 g (92%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710185B2
Source datasetuspto-grants-2004_03
ORD IDord-00d084a0718e4d45adc6d05b8ef4d1b0
Source noteuspto-grants-2004_03