HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625774Generated: October 25, 2026
2-Amino-4-(benzyloxy)benzamide → HCID 66610642, compound
https://huagongshe.com/reaction/625774
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-4-(benzyloxy)benzamide | HCID 23130277 | — |
| Reactant | 5-(4-Fluorophenyl)-1,3-dioxolane-2,4-dione | HCID 86649050 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66610642 | HCID 66610642 | 64% |
Reaction Steps
To a solution of 2-amino-4-(benzyloxy)benzamide (4.0 g, 16.5 mmol) in THF (60 mL) was added a solution of 5-(4-fluorophenyl)-1,3-dioxolane-2,4-dione (3.65 g, 18.6 mmol) from Example 16 in THF (20 mL) portionwise at rt. After heating to 63° C. for 18 h, the solution was cooled and concentrated. After addition of H2O, the solution was extracted twice with DCM. The combined organic phases were washed with brine and dried over sodium sulfate. Chromatography on silica gel eluting with 10 to 80% EtOAc/DCM afforded 4-(benzyloxy)-2-(2-(4-fluorophenyl)-2-hydroxyacetamido)benzamide as a foamy solid (4.1 g, 64%). 1H NMR (300 MHz, DMSO-d6) δ ppm 5.06 (m, 1H), 5.12 (s, 2H) 6.68-6.74 (m, 1H) 7.14-7.20 (m, 2H) 7.32-7.51 (m, 6H) 7.77 (d, J=8.85 Hz, 1H) 8.05 (br. s., 1H) 8.30 (d, J=2.64 Hz, 1H) 12.73 (s, 1H). LC-MS (ESI) m/z 392 (M−2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09308207B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-95273d2098394866812ae15a834514ec |
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| Source note | uspto-grants-2016_04 |
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