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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477914Generated: November 1, 2026

tert-Butyl 3-(4-(tert-Butoxycarbonylamino)-1H-indol-1-yl)-3-(4-chlorophenyl)pent-4-ynoate → tert-Butyl 3-(4-(tert-butoxycarbonylamino)-1H-indol-1-yl)-3-(4-chlorophenyl)pentanoate

https://huagongshe.com/reaction/1477914

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-(4-(tert-Butoxycarbonylamino)-1H-indol-1-yl)-3-(4-chlorophenyl)pent-4-ynoateHCID 86705058—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Producttert-Butyl 3-(4-(tert-butoxycarbonylamino)-1H-indol-1-yl)-3-(4-chlorophenyl)pentanoateHCID 117809455—

Reaction Steps

To a solution of the product of Step E (150 mg, 0.3 mmol) in ethanol (3 mL) was added PtO2 (6.8 mg, 0.03 mmol) at room temperature under H2 atmosphere for 2 h. The solid was filtered off and the filtrate was concentrated in vacuo to give the title compound as colorless oil. LC/MS m/z=499.2[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403807B2
Source datasetuspto-grants-2016_08
ORD IDord-fadfd6095fbe4b5d81736a6c87480d6b
Source noteuspto-grants-2016_08