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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydropyran-4-ylacetic acid | HCID 2773575 | — |
| Reactant | 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid | HCID 10988214 | — |
| Reactant | tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate | HCID 21940085 | — |
| Reactant | tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate | HCID 22181157 | — |
| Reactant | 2-Cyclopentylbenzoic acid | HCID 22763155 | — |
| Product | HCID 86702047 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975398B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-3d6b74a5f9184f31822bac2977c3b7a3 |
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| Source note | uspto-grants-2015_03 |
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