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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714347Generated: October 27, 2026

HCID 178430407, compound → HCID 178521772, compound

https://huagongshe.com/reaction/714347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178430407HCID 178430407—
ReactantHCID 178521771HCID 178521771—
ProductHCID 178521772HCID 17852177213%

Reaction Steps

Following the procedure as described in Example 10, making variations as required to replace N-(4-(4-methyl-4,5-dihydro-1H-imidazol-2-yl)pyridin-2-yl)benzamide with N-(4-(4-phenyl-4,5-dihydro-1H-imidazol-2-yl)pyridin-2-yl)benzamide, N-(4-(4-phenyl-1H-imidazol-2-yl)pyridin-2-yl)benzamide was obtained as a colorless solid in 13% yield: mp 265-267° C.; 1H NMR (300 MHz, DMSO-d6) δ 13.14 (br s, 1H), 10.88 (br s, 1H), 8.81 (s, 1H), 8.47 (d, J=5.2 Hz, 1H), 8.10-8.05 (m, 2H), 7.93-7.88 (m, 2H), 7.72 (dd, J=5.2, 1.5 Hz, 1H), 7.65-7.36 (m, 6H), 7.28-7.21 (m, 1H); 13C NMR (75 MHz, DMSO-d6) δ 165.9, 152.8, 148.5, 143.6, 141.9, 139.1, 134.1, 134.0, 131.9, 128.5, 128.4, 127.9, 126.5, 124.5, 115.8, 115.2, 110.0; MS (ES+) m/z 341.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187426B2
Source datasetuspto-grants-2015_11
ORD IDord-c9876f038e564fff958c0c1b960bc709
Source noteuspto-grants-2015_11