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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051837Generated: November 3, 2026

Diisopropylethylamine → (1-Isopropyl-7-(methylsulfonyl)-2-(4-(trifluoromethyl)pyrimidin-2-yl)-1,2,3,4-tetrahydropyrazino[1,2-a]indol-8-yl)methanol

https://huagongshe.com/reaction/1051837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-4-(trifluoromethyl)pyrimidineHCID 2773912—
Reactant8-(((Tert-butyldiphenylsilyl)oxy)methyl)-1-isopropyl-7-(methylsulfonyl)-1,2,3,4-tetrahydropyrazino[1,2-a]indoleHCID 89815906—
SolventIsopropanol methylene chlorideHCID 21966342—
Product(1-Isopropyl-7-(methylsulfonyl)-2-(4-(trifluoromethyl)pyrimidin-2-yl)-1,2,3,4-tetrahydropyrazino[1,2-a]indol-8-yl)methanolHCID 7815840572%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-chloro-4-(trifluoromethyl)pyrimidine (80 mg, 0.44 mmol), 8-(((tert-butyldiphenylsilyl)oxy)methyl)-1-isopropyl-7-(methylsulfonyl)-1,2,3,4-tetrahydropyrazino[1,2-a]indole (crude, from step 9), and DIEA (115 μL, 0.66 mmol) in i-PrOH/CH2Cl2 (2 mL/1 mL) was stirred at 110° C. for 30 h. The solvent was removed under reduced pressure and the crude residue was purified by silica chromatography and SFC separation on a chiral column to give isomers of (1-isopropyl-7-(methylsulfonyl)-2-(4-(trifluoromethyl)pyrimidin-2-yl)-1,2,3,4-tetrahydropyrazino[1,2-a]indol-8-yl)methanol (75 mg, 72% yield for two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388190B2
Source datasetuspto-grants-2016_07
ORD IDord-0c8fc9246214483da228617769aee13b
Source noteuspto-grants-2016_07