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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218147Generated: October 27, 2026

Ammonia → 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2-propyl-3-phenylpropanamide

https://huagongshe.com/reaction/218147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-((1-(4-fluorophenyl)-1H-indazol-5-yl)(phenyl)methyl)pentanoic acidHCID 59251152—
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-propyl-3-phenylpropanoyl fluorideHCID 86640191—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2-propyl-3-phenylpropanamideHCID 68705180—

Reaction Conditions

Temperature-78 °C

Reaction Steps

(c)(d) 2-((1-(4-fluorophenyl)-1H-indazol-5-yl)(phenyl)methyl)pentanoic acid (50, mg, 0.124 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-propyl-3-phenylpropanoyl fluoride (0.32 mmol) 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-propyl-3-phenylpropanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198311B2
Source datasetuspto-grants-2012_06
ORD IDord-61b8de496ff8456394e3b576c89ac3f3
Source noteuspto-grants-2012_06