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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713498Generated: November 3, 2026

2-(4-(4-Fluorobenzoyl)piperidin-1-YL)acetic acid → HCID 136237394, compound

https://huagongshe.com/reaction/713498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(4-Fluorobenzoyl)piperidin-1-YL)acetic acidHCID 71226402—
ReactantHCID 136627263HCID 136627263—
ProductHCID 136237394HCID 136237394—

Reaction Steps

Following general procedure of Example 4, the title compound was prepared (26.9 mg) from (R)-2-((1-(4-fluorophenyl)ethylamino)methyl)-7,8-dihydro-3H-pyrano[4,3-d]pyrimidin-4(5H)-one and 2-(4-(4-fluorobenzoyl)piperidin-1-yl)acetic acid. Exact mass calculated for C30H32FN4O4 550.6. found 551.4 (ESI, M+H); 1H NMR (400 MHz, dichloromethane-d2) δ ppm 7.97 (dd, J=8.84, 5.31 Hz, 2H) 7.31 (dd, J=8.59, 5.05 Hz, 1H) 7.13-7.27 (m, 3H) 6.88 (t, J=7.83 Hz, 1H) 6.03 (q, J=7.07 Hz, 1H) 4.27-4.57 (m, 5H) 4.11 (br. s., 2H) 3.85-4.03 (m, 4H) 3.36 (br. s., 1H) 3.30 (br. s., 2H) 2.97 (s, 1H) 2.70 (br. s., 2H) 2.59 (d, J=4.04 Hz, 1H) 2.12 (s, 4H) 1.68 (d, J=7.07 Hz, 1H) 1.49 (d, J=7.07 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-8bb6e35073044275a4b3c9f13b7c90ea
Source noteuspto-grants-2015_11