HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681277Generated: November 2, 2026
HCID 178420405, compound → HCID 178517572, compound
https://huagongshe.com/reaction/1681277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178420405 | HCID 178420405 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178517572 | HCID 178517572 | 97% |
Reaction Steps
A mixture of 5-benzyloxypyrrolo[3,4-b]pyridine (Compound 7f, 1.38 g, 6.15 mmol), 5% Pd/C (0.30 g), and absolute ethanol (25 mL) was shaken under a hydrogen atmosphere (3 atm) for 30 minutes. The resulting mixture was filtered through diatomaceous earth (Celite (trademark)), and the filtrate was evaporated under reduced pressure. The residual solid was triturated in ethyl ether to yield Compound 7i (0.80 g, 5.96 mmol, 97%) as an off-white crystalline solid: mp, 280.0°-282.0° C.: IR (KBr) 1,640, 1,615, 1,605, 1,455, 1,430, 1,400, 1,380, 1,365 cm-1 ; 1H NMR (DMSO-d6) δ 11.4 (br m, 2H), 7.56 (d, J=9.7 Hz, 1H), 7.16 (d, J=3.1 Hz, 1H), 6.01-5.93 (m, 2H); 13C NMR (DMSO-d6) 162.0, 131.9, 127.9, 125.0, 118.2, 112.2, 94.5; LRMS (m/z, relative intensity) 135 (41), 134 (M+, 100), 106 (66), 105 (42), 79 (59), 53 (31), 52 (52). Anal. calcd. for C7H6N2O: C, 62.68; H, 4.51; N, 20.88; found: C, 62.40; H, 4.40; N, 20.76.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05169947 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-5b75e81d8736400ab1d65fb0aeef24f8 |
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| Source note | uspto-grants-1992_12 |
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