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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709865Generated: November 1, 2026

HCID 178453525, compound → HCID 178453569, compound

https://huagongshe.com/reaction/709865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178453525HCID 178453525—
ReactantHCID 178453572HCID 178453572—
ProductHCID 178453569HCID 17845356968%

Reaction Steps

[1-[6-(trans-4-tert-Butyl-cyclohexyloxy)-5-trifluoromethyl-quinolin-2-yl]-2-(di-tert-butoxy-phosphoryloxy)-1-methyl-ethyl]-carbamic acid tert-butyl ester Enantiomer 1 was synthesized as per [1-[6-(trans-4-tert-Butyl-cyclohexyloxy)-quinolin-2-yl]-2-(di-tert-butoxy-phosphoryloxy)-1-methyl-ethyl]-carbamic acid tert-butyl ester Enantiomer 1 (Example 29) in 68% yield using {1-[6-(trans-4-tert-Butyl-cyclohexyloxy)-5-trifluoromethyl-quinolin-2-yl]-2-hydroxy-1-methyl-ethyl}-carbamic acid tert-butyl ester Enantiomer 1 as starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181191B2
Source datasetuspto-grants-2015_11
ORD IDord-d048ab25950d415295e9938454adb81e
Source noteuspto-grants-2015_11