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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714332Generated: October 29, 2026

2-Fluorobenzoyl chloride → HCID 67153850, compound

https://huagongshe.com/reaction/714332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
Reactant2-amino-N-benzylisonicotinamideHCID 18752897—
ProductHCID 67153850HCID 6715385080%

Reaction Steps

Following the procedure as describe in Example 6, making non-critical variations as required to replace 2-fluorobenzoyl chloride with 3-(trifluoromethyl)benzoyl chloride to react with 2-amino-N-benzylisonicotinamide, N-benzyl-2-(3-(trifluoromethyl)benzamido)-isonicotinamide was obtained as a colorless solid in 80% yield: mp 126-128° C.; 1H NMR (300 MHz, CDCl3) δ 10.36 (s, 1H), 8.82 (s, 1H), 8.41-8.14 (m, 4H), 7.95-7.27 (m, 7H), 7.03 (s, 1H), 4.57 (d, J=5.1 Hz, 2H); MS (ES+) m/z 400.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187426B2
Source datasetuspto-grants-2015_11
ORD IDord-7b8475104b3c4cf8842381806bd70b0f
Source noteuspto-grants-2015_11