Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864799Generated: October 31, 2026

Acetic Acid → 5-{4-Fluoro-3-[(3-pyrrolidin-1-yl-propylamino)-methyl]-phenyl}-indazole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1864799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-PyrrolidinepropanamineHCID 31670—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(4-Fluoro-3-formylphenyl)-indazole-1-carboxylic acid tert-butyl esterHCID 86616469—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product5-{4-Fluoro-3-[(3-pyrrolidin-1-yl-propylamino)-methyl]-phenyl}-indazole-1-carboxylic acid tert-butyl esterHCID 6875057299.1%

Reaction Steps

Sodium triacetoxyborohydride (190 mg, 0.88 mmol) was added to a mixture of 5-(4-fluoro-3-formylphenyl)-indazole-1-carboxylic acid tert-butyl ester (100 mg, 0.29 mmol) and N-(3-aminopropyl)pyrrolidine (74 mg, 0.59 mmol) and acetic acid (105 mg, 1.8 mmol) in dichloroethane. The mixture was stirred at ambient temperature overnight, and then it was diluted with dichloromethane and washed with 1 M sodium carbonate solution. The layers were separated and the aqueous phase extracted with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered and concentrated to leave the crude product. Chromatography (elution with methanol/dichloromethane) provided 130 mg of product. LC/MS: Retention time, 1.98 min; (M+H)=453.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625889B2
Source datasetuspto-grants-2009_12
ORD IDord-27e26f2df4c541639c419bc5f2e8911b
Source noteuspto-grants-2009_12