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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39426Generated: October 25, 2026

Acetic Acid → trans-(4-Cyclopentylamino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/39426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopentanoneHCID 8452—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-Butyl ((3S,4R)-4-aminotetrahydro-2H-pyran-3-yl)carbamateHCID 67358958—
SolventMethanolHCID 887—
Producttrans-(4-Cyclopentylamino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl esterHCID 6735895362%

Reaction Conditions

Temperature45 °C

Reaction Steps

trans-(4-Amino-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester (intermediate G, 1.0 g, 4.63 mmol) was dissolved in 90 mL methanol. Acetic acid (1.4 g, 23 mmol) and cyclopentanone (1.18 g, 14 mmol) were added and the reaction mixture was stirred at 45° C. overnight. Sodium cyanoborohydride (612 mg, 9.7 mmol) was added and stirring was continued at 45° C. for 2 h. The mixture was extracted with 2N sodium carbonate solution and ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (dichloromethane/methanol/ammonia 100:0:0→90:10:1) yielded the title compound as a yellow solid (815 mg, 62%), MS: m/e=229.4 [(M-butene)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524909B2
Source datasetuspto-grants-2013_09
ORD IDord-f6d13372ecf343bda0ef3a8ece003fbc
Source noteuspto-grants-2013_09