HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528882Generated: October 29, 2026
Phosphorus oxychloride → HCID 71086349, compound
https://huagongshe.com/reaction/528882
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | (2-Methoxyethyl)(methyl)amine | HCID 300977 | — |
| Reactant | HCID 14198414 | HCID 14198414 | — |
| Product | HCID 71086349 | HCID 71086349 | 28.9% |
Reaction Steps
A mixture of 4,5-dihydro-1H-benzo[e][1,3]diazepin-3(2H)-one (Boyer, J. H. et al., J. Chem. Soc., Perkin Trans. I, 2137-2140 (1988)) (70 mg, 0.43 mmol) and POCl3 (805 μL, 8.63 mmol) was heated at 106° C. for 2 h. The reaction mixture was then concentrated in vacuo, dissolved in CHCl3 and azeotroped with PhMe. The residue was dissolved in THF (1.0 mL) and treated with 2-methoxy-N-methylethanamine (70 μl, 0.65 mmol). The resulting reaction mixture was stirred at room temperature overnight and then concentrated in vacuo. The residue was purified by preparative HPLC to give the title compound (29 mg, 28%). 1H NMR (CDCl3) δ 7.38-7.31 (m, 2H), 7.31-7.21 (m, 2H), 5.95 (br s, 1H), 4.61 (d, J=4.6 Hz, 2H), 4.39 (d, J=4.6 Hz, 2H), 3.56-3.51 (m, 2H), 3.42 (s, 3H), 3.40-3.36 (m, 2H), 3.10 (s, 3H); MS(ESI+) m/z 234.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346795B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-1f22802d31944ab8b898e5988eba0745 |
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| Source note | uspto-grants-2016_05 |
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