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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853875Generated: October 30, 2026

Water → 2,2-dimethyl-3-[2'-oxo-5'-(pyrrolidin-1-ylsulfonyl)spiro[1,3-dioxane-2,3'-indol]-1'(2'H)-yl]propanenitrile

https://huagongshe.com/reaction/853875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Chloro-2,2-dimethylpropanenitrileHCID 14713915—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5'-(pyrrolidin-1-ylsulfonyl)spiro[1,3-dioxane-2,3'-indol]-2'(1'H)-oneHCID 58932571—
SolventDimethyl SulfoxideHCID 679—
Product2,2-dimethyl-3-[2'-oxo-5'-(pyrrolidin-1-ylsulfonyl)spiro[1,3-dioxane-2,3'-indol]-1'(2'H)-yl]propanenitrileHCID 5893257577%

Reaction Conditions

Temperature130 °C

Reaction Steps

At room temperature, to a stirred solution of potassium t-butoxide (0.287 g, 2.56 mmol, 1.2 eq) in anhydrous DMSO (4 mL) was added 5′-(pyrrolidin-1-ylsulfonyl)spiro[1,3-dioxane-2,3′-indol]-2′(1′H)-one (0.72 g, 2.13 mmol). After stirring 20 minutes, 3-chloro-2,2-dimethylpropionitrile (3 eq) was added drop-wise and the reaction was heated at 130° C. for 20 hr. The reaction mixture was heated at 126° C. for 16 h. After cooling to room temperature, the reaction was poured into H2O (100 mL) and extracted with Et2O (3×). The combined organic extracts were dried over Na2SO4, filtered and concentrated. The crude product was purified on Biotage KP silica gel eluting with CH2Cl2/CH3OH H4OH (97/2/1) followed by a second chromatography eluting with 50/50 Pet. ether/EtOAc to give the title compound as a white solid (0.69 g, 77% yield). NMR: consistent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256198B2
Source datasetuspto-grants-2007_08
ORD IDord-15883286c48a40f69b8e82f062f608fd
Source noteuspto-grants-2007_08