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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205676Generated: November 1, 2026

Tetrahydrofuran → HCID 71548046, compound

https://huagongshe.com/reaction/2205676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHexanoyl chlorideHCID 67340—
ReactantHCID 89488324HCID 89488324—
SolventEthyl AcetateHCID 8857—
ProductHCID 71548046HCID 7154804666.5%

Reaction Steps

To a solution of (6S,9S)—N-benzyl-6-(4-hydroxybenzyl)-9-methyl-8-(naphthalen-1-ylmethyl)-4,7-dioxooctahydro-1H-pyrazino[1,2-a]pyrimidine-1-carboxamide 60 mg (0.106 mmol) in dry-THF (2 ml), hexanoyl chloride 44 μl (0.319 mmol) and then triethylamine 45 μl (0.319 mmol) were added and stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate (10 ml) and washed with water (10 ml), saturated sodium bicarbonate (10 ml), water (10 ml), and brine (10 ml). The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue was purified by Büchi silica gel column chromatography (chloroform:methanol=99:1 to 98:2) to obtain title compound 46.6 mg (66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371330B2
Source datasetuspto-grants-2016_06
ORD IDord-0ce651f947f3447499648101af1fe25f
Source noteuspto-grants-2016_06