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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681277Generated: November 2, 2026

HCID 178420405, compound → HCID 178517572, compound

https://huagongshe.com/reaction/1681277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178420405HCID 178420405—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178517572HCID 17851757297%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169947
Source datasetuspto-grants-1992_12
ORD IDord-5b75e81d8736400ab1d65fb0aeef24f8
Source noteuspto-grants-1992_12