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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911062Generated: November 1, 2026

Diisopropylethylamine → HCID 59708480, compound

https://huagongshe.com/reaction/1911062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-2-[4-(4-chloro-phenyl)-piperazin-1-yl]-6,7-dihydro-thieno[3,2-d]pyrimidine 5-oxideHCID 59475895—
ReactantHCID 131729446HCID 131729446—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59708480HCID 59708480—

Reaction Conditions

Temperature120 °C

Reaction Steps

350 mg 4-chloro-2-[4-(4-chloro-phenyl)-piperazin-1-yl]-6,7-dihydro-thieno[3,2-d]pyrimidine 5-oxide (cf Example 124), 600 mg (R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-ethylamine and 350 μl diisopropylethylamine are placed in 4 ml dioxane, heated to 120° C. in the microwave for 0.2 hours. Then the reaction mixture is evaporated to dryness. The residue is suspended in water/acetonitrile/trifluoroacetic acid and stirred for 3 hours at ambient temperature. The reaction mixture is evaporated to dryness and the diastereomers are separated by preparative HPLC (method D). Analytical HPLC-MS (method E): Diastereomer 1: RT=1.20 min; Diastereomer 2: RT=1.25 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604039B2
Source datasetuspto-grants-2013_12
ORD IDord-50d947f3cf99404c836545e2b310a871
Source noteuspto-grants-2013_12