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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33599Generated: October 28, 2026

tert-Butanol → N-[5-(N-tert-butoxycarbonylsulfamoylamino)-4,6-dimethyl-1-octylindolin-7-yl]-2,2-dimethylpropanamide

https://huagongshe.com/reaction/33599

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantN-(5-Amino-4,6-dimethyl-1-octylindolin-7-yl)-2,2-dimethylpropanamideHCID 23075425—
SolventDichloromethaneHCID 6344—
ProductN-[5-(N-tert-butoxycarbonylsulfamoylamino)-4,6-dimethyl-1-octylindolin-7-yl]-2,2-dimethylpropanamideHCID 23075439—

Reaction Steps

tert-Butanol (0.85 mL) was dissolved in methylene chloride (17 mL) and chlorosulfonyl isocyanate (0.77 mL) was added at −18° C. The mixture was stirred at the same temperature for 30 min and N-(5-amino-4,6-dimethyl-1-octylindolin-7-yl)-2,2-dimethylpropanamide (1.66 g) and triethylamine (1.24 mL) were added. The mixture was further stirred at −5° C. for 30 min. Methylene chloride (50 mL) was added, and the mixture was washed successively with 10% aqueous citric acid, saturated aqueous sodium hydrogencarbonate, and then saturated brine (50 mL) and dried over sodium sulfate. Then, methylene chloride was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as crystals (1.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429612B2
Source datasetuspto-grants-2008_09
ORD IDord-bb2f4849cf9745ecbfbe67d605536b76
Source noteuspto-grants-2008_09