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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873570Generated: October 26, 2026

Tetrahydropyran-4-ylacetic acid → HCID 86702047, compound

https://huagongshe.com/reaction/873570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydropyran-4-ylacetic acidHCID 2773575—
Reactant1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acidHCID 10988214—
Reactanttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 21940085—
Reactanttert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylateHCID 22181157—
Reactant2-Cyclopentylbenzoic acidHCID 22763155—
ProductHCID 86702047HCID 86702047—

Reaction Steps

The title compound was prepared as described in Example 1, substituting (S)-1-((benzyloxy)carbonyl)pyrrolidine-3-carboxylic acid for 1-(benzyloxycarbonyl)azetidine-3-carboxylic acid and tert-butyl 4-(4-aminophenyl)piperidine-1-carboxylate for tert-butyl 4-(4-aminophenoxy)piperidine-1-carboxylate in Example 1A, and cyclopentylbenzoic acid for 2-(tetrahydro-2H-pyran-4-yl)acetic acid in Example 1E. 1H NMR (300 MHz, DMSO-d6) δ ppm 10.03 (s, 1H), 7.95 (d, J=2.8 Hz, 1H), 7.85 (dd, J=4.6, 1.2 Hz, 1H), 7.55 (t, J=10.1 Hz, 2H), 7.16 (dd, J=8.3, 4.3 Hz, 3H), 6.92 (ddd, J=8.4, 2.9, 1.3 Hz, 1H), 4.54 (d, J=12.7 Hz, 1H), 3.98 (d, J=13.7 Hz, 1H), 3.64-3.48 (m, 1H), 3.48-3.38 (m, 1H), 3.22-2.87 (m, 2H), 2.68 (dd, J=24.3, 12.3 Hz, 1H), 2.41-2.01 (m, 6H), 1.77 (s, 4H), 1.68-1.04 (m, 9H); MS (ESI(+)) m/e 461 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975398B2
Source datasetuspto-grants-2015_03
ORD IDord-3d6b74a5f9184f31822bac2977c3b7a3
Source noteuspto-grants-2015_03