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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,2-dimethyl-3-phenylpropan-1-amine | HCID 59251172 | — |
| Reactant | 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoic acid | HCID 59251185 | — |
| Product | 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanamide | HCID 68703811 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198311B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-169dcecb6415471fad0dc815d2e3fd9e |
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| Source note | uspto-grants-2012_06 |
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