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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037970Generated: November 3, 2026

O-(Tetrahydropyran-2-yl)hydroxylamine → HCID 58418151, compound

https://huagongshe.com/reaction/1037970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(Tetrahydropyran-2-yl)hydroxylamineHCID 5142091—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 58418192HCID 58418192—
SolventDimethylformamideHCID 6228—
ProductHCID 58418151HCID 58418151—

Reaction Steps

To the crude (R)-3-(1-(benzofuran-2-carboxamido)ethyl)isoxazole-5-carboxylic acid in a microwave vial was added HATU (0.0544 g, 0.143 mmol), TEA (0.087 g, 0.858 mmol) in DMF (1.0 mL), followed by O-(tetrahydropyran-2-yl)hydroxylamine (0.0335 g, 0.286 mmol) in DMF (1.0 mL). The mixture was shaken at rt for 16 h, then the solvent was evaporated. To the residue was added THF (2.0 mL) and hydrochloric acid (0.0715 mL, 4.0 M in 1,4-dioxane). After shaking at rt for 1 h, the solvent was evaporated. To the residue was added DMSO (1.2 mL). After filtration, the solution was purified by prep-HPLC to give ((R)-3-(1-(benzofuran-2-carboxamido)ethyl)-N-hydroxyisoxazole-5-carboxamide. LC-MS: (FA) ES+ 347.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546588B2
Source datasetuspto-grants-2013_10
ORD IDord-709928f6879b4f66bc88a756aac06553
Source noteuspto-grants-2013_10