HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32977Generated: October 26, 2026
Dimethylformamide → HCID 67011482, compound
https://huagongshe.com/reaction/32977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | (2-{-4-[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-2-methyl-but-2-enylamino}-ethyl)-phosphonic acid diethyl ester | HCID 76541029 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67011482 | HCID 67011482 | 36.8% |
Reaction Steps
A solution of (2-{4-[6-methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-2-methyl-but-2-enylamino}-ethyl)-phosphonic acid diethyl ester (30 mg, 0.055 mmol), TMSBr (72 μL, 0.55 mmol), and 2,6-lutidine (64 μL, 0.55 mmol) was stirred in CH2Cl2 (1 mL) and DMF (0.5 mL) for 1 hour at ambient temperature. The reaction mixture was purified by RP HPLC using a C18 column with a gradient of H2O, 0.1% TFA-acetonitrile, 0.1% TFA to provide 7.8 mg of the product as a white solid. 1H NMR (300 MHz, CD3OD) δ 1.96 (s, 3H), 1.95-2.07 (m, 2H), 2.16 (s, 3H), 3.10-3.24 (m, 2H), 3.51 (d, 2H, J=7 Hz), 3.57 (s, 2H), 3.81 (s, 3H), 5.25 (s, 2H), 5.73 (t, 1H, J=7 Hz) ppm; 31P (121.4 MHz, CD3OD) δ 20.2 ppm; 19F NMR (282.6 MHz, CD3OD) δ-74.0 ppm; MS (m/z) 386.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07427636B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-6e3a2d46b07b4f9a8b151dd9a654820e |
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| Source note | uspto-grants-2008_09 |
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