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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427282Generated: November 2, 2026

tert-butyl 1-(3-(4-chlorophenyl)-5,5,5-trifluoropent-1-yn-3-yl)-1H-indazol-4-ylcarbamate → tert-butyl 1-(3-(4-chlorophenyl)-1,1,1-trifluoropentan-3-yl)-1H-indazol-4-ylcarbamate

https://huagongshe.com/reaction/1427282

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 1-(3-(4-chlorophenyl)-5,5,5-trifluoropent-1-yn-3-yl)-1H-indazol-4-ylcarbamateHCID 86705055—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Producttert-butyl 1-(3-(4-chlorophenyl)-1,1,1-trifluoropentan-3-yl)-1H-indazol-4-ylcarbamateHCID 70586827—

Reaction Steps

To a solution of the product of Step D (100 mg, 0.21 mmol) in ethanol (3 mL) was added PtO2 (10 mg, 0.044 mmol) at room temperature under H2 atmosphere for 2 h. The solid was filtered off and filtrate was concentrated in vacuo to obtain the title compound as colorless oil. LC/MS m/z=468.1[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933113B2
Source datasetuspto-grants-2015_01
ORD IDord-f4d81fd7f9a747e5b1bbb83091702b48
Source noteuspto-grants-2015_01