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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25720Generated: October 29, 2026

Tetrahydrofuran → HCID 59065917, compound

https://huagongshe.com/reaction/25720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantbenzyl (1S)-1-methyl-2-oxo-2-[(3-oxopropyl)amino]ethylcarbamateHCID 59065906—
ReactantHCID 59065937HCID 59065937—
CatalystAcetic AcidHCID 176—
ProductHCID 59065917HCID 5906591739%

Reaction Steps

By using an analogous procedure to that described for Example 1, a solution of tert-(4-methoxybenzyl)-2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl)-tetrahydro-2-furanyl]-3-hydroxypropanoate (80 mg, 0.111 mmol, obtained from Reference Example 6), benzyl (1S)-1-methyl-2-oxo-2-[(3-oxopropyl)amino]ethylcarbamate (39 mg, 0.139 mmol, obtained from Reference Example 20), acetic acid (1 drop), and sodium triacetoxyborohydride (47 mg, 0.222 mmol) in anhydrous tetrahydrofuran (4 ml) was stirred at room temperature under nitrogen for 3 hours. The product was purified by chromatography (flash column, silica gel, 5% methanol in methylene chloride) to provide tert-butyl (5S,12S)-12-[(R)-[(3R,4R,5R)-3,4-bis{[tert-butyl(dimethyl)silyl]oxy}-5-(3-(4-methoxybenzyl)-2,4-dioxo-3,4-dihydro-1(2H )-pyrimidinyl)tetrahydro-2-furanyl](hydroxy)methyl]-5-methyl-3,6-dioxo-1-phenyl-2-oxa-4,7,11-triazatridecan-13-oate (43 mg, 39%) as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858591B2
Source datasetuspto-grants-2005_02
ORD IDord-012974ea7b924d48b288baf598a885fc
Source noteuspto-grants-2005_02