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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489628Generated: October 30, 2026

(S)-3-tert-Butoxycarbonylamino-2-hydroxy-pentanoic acid → (S)-2-Amino-1-(3-cyclopropyl-1,2,4-oxadiazol-5-yl)-butan-1-ol

https://huagongshe.com/reaction/489628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-tert-Butoxycarbonylamino-2-hydroxy-pentanoic acidHCID 86588337—
ReactantHCID 178513214HCID 178513214—
SolventDichloromethaneHCID 6344—
Product(S)-2-Amino-1-(3-cyclopropyl-1,2,4-oxadiazol-5-yl)-butan-1-olHCID 68820972—

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of (S)-3-tert-Butoxycarbonylamino-2-hydroxy-pentanoic acid (2.00 g, 8.57 mmol) and N-hydroxy-cyclopropanecarboxamidine (1.03 g, 10.29 mmol) in dichloromethane (20 mL) was stirred at 0° C. and 1.25 equivalents of N-cyclohexylcarbodiimide-N′-methyl polystyrene (1.70 mmol/g, 6.30 g, 10.72 mmol) was added in portions. The reaction mixture stirred under nitrogen for three hours while warming to 15° C. The reaction mixture was filtered, the resin washed with dichloromethane and the filtrate evaporated under vacuum to dryness. [LC/MS m/z=338 (M+H+Na)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977256B2
Source datasetuspto-grants-2005_12
ORD IDord-cbb7cae2aa0c4e69a8ae41cce5ad3108
Source noteuspto-grants-2005_12