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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077073Generated: October 30, 2026

4-Amino-3-fluorobenzamide → 3-Fluoro-4-({4-[({2-[methyl(methylsulfonyl)amino]pyridin-3-yl}methyl)amino]-5-(trifluoromethyl)pyrimidin-2-yl}amino)benzamide formic acid salt

https://huagongshe.com/reaction/2077073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-fluorobenzamideHCID 12118053—
Reactant2-Fluoro-4-({-4-[({2-[methyl(methylsulfonyl)amino]pyridin-3-yl}methyl)amino]-5-(trifluoromethyl)pyrimidin-2-yl}amino)benzamide formic acid saltHCID 25117127—
SolventFormic AcidHCID 284—
Product3-Fluoro-4-({4-[({2-[methyl(methylsulfonyl)amino]pyridin-3-yl}methyl)amino]-5-(trifluoromethyl)pyrimidin-2-yl}amino)benzamide formic acid saltHCID 25117346—

Reaction Steps

Compound 14 was prepared in a manner similar to that described Example 13 for the preparation of 13 except that 4-amino-3-fluorobenzamide (1.5 equ/189 μM) was used instead of 4-amino-2-fluorobenzamide to provide the formic acid salt of 14 as a cream colored solid. Yield: 26 mg, 37%. LC-MS M+1=514. NMR (d6-DMSO) : 2.98 (3H, s), 3.09 (3H, s), 4.65 (2H, s), 7.35-7.66 (7H, m), 7.87 (1H, s), 8.23 (1H, s), 8.38 (1H, s), 9.19 (1H, s). FAK IC50: <0.000595 μM (Table 1, Example 322)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928109B2
Source datasetuspto-grants-2011_04
ORD IDord-af0ed3cfe5cd45b0b2028126a990e653
Source noteuspto-grants-2011_04