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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Bis(trimethylsilyl)trifluoroacetamide | HCID 65279 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | [(2-Bromo-4-{[(3,4-dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amino]-methyl}-phenyl)-difluoro-methyl]-phosphonic acid diethyl ester | HCID 86607370 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(2-Bromo-4-{[(3,4-dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amino]-methyl}-phenyl)-difluoro-methyl]-phosphonic acid | HCID 11556324 | 199.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381736B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-538367c3cbcb4e15b5ce81c02c08a4bb |
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| Source note | uspto-grants-2008_06 |
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