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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713503Generated: November 1, 2026

2-(4-(4-Fluorobenzoyl)piperidin-1-YL)acetic acid → HCID 136237408, compound

https://huagongshe.com/reaction/713503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(4-Fluorobenzoyl)piperidin-1-YL)acetic acidHCID 71226402—
ReactantHCID 136627222HCID 136627222—
ProductHCID 136237408HCID 136237408—

Reaction Steps

Following general procedure of Example 4, the title compound was prepared (9 mg) from (R)-2-((1-cyclopropylethylamino)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 C27H33FN4O4 496.6. found 497.6 (ESI, M+H); 1H NMR (400 MHz, DMSO-d6) δ ppm 7.98-8.21 (m, 2H) 7.40 (t, J=8.84 Hz, 2H) 4.25-4.54 (m, 5H) 3.84 (ddd, J=17.31, 5.56, 5.43 Hz, 3H) 3.70 (d, J=6.06 Hz, 1H) 3.56 (br. s., 2H) 3.23 (br. s., 1H) 2.99-3.20 (m, 2H) 1.99 (br. s., 4H) 1.00-1.29 (m, 4H) 0.68-0.94 (m, 1H) 0.46-0.68 (m, 1H) 0.38 (d, J=5.05 Hz, 1H) 0.24-0.34 (m, 1H) 0.15-0.24 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-e7389af641ad41a795154bbb206342c7
Source noteuspto-grants-2015_11