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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203178Generated: October 31, 2026

Diisopropylethylamine → 2-(5-Chloro-1-isobutyl-indazol-7-yl)acetonitrile

https://huagongshe.com/reaction/2203178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanesulfonic anhydrideHCID 81560—
Reactant(5-Chloro-1-isobutyl-1H-indazole-7-yl)-methanolHCID 118251601—
SolventDichloromethaneHCID 6344—
Product2-(5-Chloro-1-isobutyl-indazol-7-yl)acetonitrileHCID 118251649—

Reaction Steps

To a solution of compound 17 (1 g, 4.2 mmol), at room temperature and under nitrogen atmosphere, in dry dichloromethane (10 mL) were added DIPEA (0.8 mL, 4.62 mmol) and methane sulfonic anhydride. (0.8 g, 4.62 mmol) The resulting mixture was stirred for 2 h. Then, the reaction mixture was quenched with water and the mixture was extracted with more dichloromethane. The organic layer was separated, washed with Brine, dried (MgSO4), filtered and the solvent evaporated to give the desired product as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365569B2
Source datasetuspto-grants-2016_06
ORD IDord-7be3b221fdc040d19b85737e88ef271d
Source noteuspto-grants-2016_06