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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096879Generated: November 1, 2026

7-{3-[3-(4-Chloro-3,5-dimethylphenoxy)propyl]isoxazol-5-yl}-6-[cyclopropyl-(2,3-dichlorobenzyl)carbamoyl]-3,9-diazabicyclo[3.3.1]non-6-ene-3,9-dicarboxylic acid di-tert-butyl ester → 7-{3-[3-(4-Chloro-3,5-dimethylphenoxy)propyl]isoxazol-5-yl}-3,9-diaza-bicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(2,3-dichlorobenzyl)-amide

https://huagongshe.com/reaction/1096879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-{3-[3-(4-Chloro-3,5-dimethylphenoxy)propyl]isoxazol-5-yl}-6-[cyclopropyl-(2,3-dichlorobenzyl)carbamoyl]-3,9-diazabicyclo[3.3.1]non-6-ene-3,9-dicarboxylic acid di-tert-butyl esterHCID 68571289—
ReactantTrichloro-tert-butylcarbamateHCID 131729530—
CatalystZincHCID 23994—
SolventAcetic acid tetrahydrofuranHCID 23444217—
Product7-{3-[3-(4-Chloro-3,5-dimethylphenoxy)propyl]isoxazol-5-yl}-3,9-diaza-bicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(2,3-dichlorobenzyl)-amideHCID 68571189—

Reaction Steps

This compound is prepared from compound F15, according to the above-described procedure B. After cleaving the Boc-group the trichloro-tert-butylcarbamate was cleaved using Zn-powder in THF/AcOH 3:1. LC-MS: tR=0.93 min; ES+: 629.33.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138340B2
Source datasetuspto-grants-2012_03
ORD IDord-fd209ccb37c343ce84d6f4fcc9d5aa1d
Source noteuspto-grants-2012_03