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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661477Generated: October 31, 2026

Triethylamine → Cyclopropanesulfonic acid N-{1-[6-methoxypyridin-3-yl]-1-[(1-pyridin-2-yl-1H-indazol-5-yl)oxy]propan-2-yl}amide

https://huagongshe.com/reaction/1661477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantCyclopropanesulfonyl chlorideHCID 2760919—
Reactant1-[6-Methoxypyridin-3-yl]-1-[1-(pyridin-2-yl)indazol-5-yl]oxypropan-2-amineHCID 59786569—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductCyclopropanesulfonic acid N-{1-[6-methoxypyridin-3-yl]-1-[(1-pyridin-2-yl-1H-indazol-5-yl)oxy]propan-2-yl}amideHCID 24955653—

Reaction Steps

To a stirred solution of 1-[6-methoxypyridin-3-yl]-1-[1-(pyridin-2-yl)indazol-5-yl]oxypropan-2-amine (50 mg, 130 μmol) in dichloromethane (5 mL) was added triethylamine (44 μl), followed by cyclopropane sulfonic acid chloride (28 mg, 200 μmol) and DMAP (1.6 mg, 13 μmol).The stirring was continued for 20 min at room temp The reaction mixture was poured into sat. NH4Cl solution and extracted with dichloromethane then the solvent was removed i.vac., and the product purified by chromatography on silica gel. Yield 24 mg as a racemic mixture of two diastereomeres (37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030340B2
Source datasetuspto-grants-2011_10
ORD IDord-c52e4aeaaf99446c82eba58b57840406
Source noteuspto-grants-2011_10