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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710388Generated: October 30, 2026

tert-Butyl 2,2-dimethyl-5-((4-octylphenylamino)methyl)-1,3-dioxan-5-ylcarbamate → 2-Amino-2-((6-((2'-(trifluoromethyl)biphenyl-4-yl)methoxy)-3,4-dihydroisoquinolin-2(1H)-yl)methyl)propane-1,3-diol

https://huagongshe.com/reaction/710388

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 2,2-dimethyl-5-((4-octylphenylamino)methyl)-1,3-dioxan-5-ylcarbamateHCID 66726563—
Reactanttert-Butyl 2,2-dimethyl-5-((6-((2'-(trifluoromethyl)biphenyl-4-yl)methoxy)-3,4-dihydroisoquinolin-2(1H)-yl)methyl)-1,3-dioxan-5-ylcarbamateHCID 86661789—
Product2-Amino-2-((6-((2'-(trifluoromethyl)biphenyl-4-yl)methoxy)-3,4-dihydroisoquinolin-2(1H)-yl)methyl)propane-1,3-diolHCID 4619602275%

Reaction Steps

When the product of Step C was substituted for tert-butyl 2,2-dimethyl-5-((4-octylphenylamino)methyl)-1,3-dioxan-5-ylcarbamate in Example 1, Step B, the identical process afforded the title compound in 75% yield, as an off white solid. 1H-NMR (CDCl3+CD3OD) 2.5-3.9 (m, 16H+H2O); 5.02 (s, 2H); 6.69-6.91 (m, 3H); 7.25-7.53 (m, 7H); 7.68 (d, 1H, J=7.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181182B2
Source datasetuspto-grants-2015_11
ORD IDord-bda90ea171e14a6995c69a73bc5978d9
Source noteuspto-grants-2015_11