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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714367Generated: October 29, 2026

1-[2-(Trifluoromethyl)-1,3-thiazol-4-yl]methanamine → HCID 44552916, compound

https://huagongshe.com/reaction/714367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-(Trifluoromethyl)-1,3-thiazol-4-yl]methanamineHCID 17750415—
Reactant1,3-Oxazol-4-ylmethanamineHCID 23055690—
Reactant2-(3-(4-Fluorobenzyl)-2-oxoimidazolidin-1-yl)isonicotinic acidHCID 58247791—
ProductHCID 44552916HCID 4455291630%

Reaction Steps

Following the procedure as described in Example 14, making variations as required to replace oxazol-4-ylmethanamine with (2-(trifluoromethyl)thiazol-4-yl)methanamine to react with 2-(3-(4-fluorobenzyl)-2-oxoimidazolidin-1-yl)isonicotinic acid, 2-(3-(4-fluorobenzyl)-2-oxoimidazolidin-1-yl)-N-((2-(trifluoromethyl)thiazol-4-yl)methyl)isonicotinamide was obtained as a colorless solid in 30% yield: mp 66-68° C.; 1H NMR (300 MHz, CDCl3) δ 8.68 (s, 1H), 8.36 (d, J=5.1 Hz, 1H), 7.59 (s, 1H), 7.35 (d, J=5.1 Hz, 1H), 7.28-7.20 (m, 2H), 7.17-6.99 (m, 3H), 4.78 (d, J=6.0 Hz, 2H), 4.43 (s, 2H), 4.03 (t, J=8.0 Hz, 2H), 3.37 (t, J=8.0 Hz, 2H); MS (ES+) m/z 479.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187426B2
Source datasetuspto-grants-2015_11
ORD IDord-0cf6f68c99b34a8f9514fc260ddb65c6
Source noteuspto-grants-2015_11