Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218151Generated: October 28, 2026

3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,2-dimethyl-3-phenylpropan-1-amine → 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanamide

https://huagongshe.com/reaction/218151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,2-dimethyl-3-phenylpropan-1-amineHCID 59251172—
Reactant3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoic acidHCID 59251185—
Product3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanamideHCID 68703811—

Reaction Conditions

Temperature-78 °C

Reaction Steps

(c)(d) 3-(1-(4-Fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoic acid (80, mg, 0.154 mmol) was converted into the acid fluoride using the identical procedure to that for Synthetic Intermediate I above. A solution of 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoyl fluoride in anhydrous THF (5 mL) at −78° C. was bubbled NH3 (g) for 10 minutes. The reaction mixture was sealed and stirred at −78° C. for 15 min and at rt for 1 hr. Water (100 mL) was added, the reaction mixture was extracted with ethyl acetate (100 mL), dried (Na2SO4), and concentrated to give 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropan-amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198311B2
Source datasetuspto-grants-2012_06
ORD IDord-169dcecb6415471fad0dc815d2e3fd9e
Source noteuspto-grants-2012_06