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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130352Generated: October 30, 2026

N,N-Bis(trimethylsilyl)trifluoroacetamide → [(2-Bromo-4-{[(3,4-dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amino]-methyl}-phenyl)-difluoro-methyl]-phosphonic acid

https://huagongshe.com/reaction/130352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Bis(trimethylsilyl)trifluoroacetamideHCID 65279—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant[(2-Bromo-4-{[(3,4-dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amino]-methyl}-phenyl)-difluoro-methyl]-phosphonic acid diethyl esterHCID 86607370—
SolventDichloromethaneHCID 6344—
Product[(2-Bromo-4-{[(3,4-dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amino]-methyl}-phenyl)-difluoro-methyl]-phosphonic acidHCID 11556324199.9%

Reaction Steps

To [(2-bromo-4-{[(3,4-dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amino]-methyl}-phenyl)-difluoro-methyl]-phosphonic acid diethyl ester (0.176 g, 0.25 mmol) in CH2Cl2 (3 mL) was added bistrimethylsilyltrifluoroacetamide (0.66 g, 2.59 mmol) and reaction mixture was stirred at room temperature for 1 h after which the reaction mixture is cooled to 20° C. and iodotrimethylsilane (0.51 g, 2.59 mmol) is added drop wise. The resulting mixture was stirred at room temperature for 1.5 hours, after which it was concentrated in vacuo. The resulting material was stirred in CH3CN (4 mL), H2O (0.5 mL), and TFA (0.5 mL) for 0.5 hours, after which it was concentrated in vacuo and partitioned between ethyl acetate and acidic Na2S2O4. The organic layer was dried over MgSO4 and concentrated in vacuo to yield 0.31 g (99%) of a white foam; 1H NMR (300 MHz, DMSO-d6) δ 7.99-7.28 (m, 12 H), 5.33 (s, 2 H); LCMS m/z 619 [M−]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381736B2
Source datasetuspto-grants-2008_06
ORD IDord-538367c3cbcb4e15b5ce81c02c08a4bb
Source noteuspto-grants-2008_06