HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645265Generated: October 29, 2026
HCID 59263325, compound → HCID 11998467, compound
https://huagongshe.com/reaction/645265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59263325 | HCID 59263325 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11998467 | HCID 11998467 | 98% |
Reaction Steps
A suspension of 1′-[3-(benzyloxy)propyl]spiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-2′(1′H)-one (6.27 g, 14.5 mmol) and 10% Pd/C (0.5 g) in MeOH (150 mL) was hydrogenated under the normal pressure of hydrogen overnight and filtered through a pad of celite. The filtrate was concentrated in vacuo to dryness. The residue was crystallized from ether to yield the title compound (4.82 g) as a white solid in 98% yield: 1H NMR (300 MHz, CDCl3) δ 7.38-6.93 (m, 4H), 6.49 (s, 1H), 6.10 (s, 1H), 4.87 (m, 1H), 4.63 (m, 1H), 4.01-3.81 (m, 2H), 3.62 (t, 2H), 2.89 (br, 1H), 1.99-1.91(m, 2H); 13C NMR (75 MHz, CDCl3) δ 178.8, 156.0, 148.9, 142.4, 142.1, 132.3, 129.0, 128.9, 124.1, 123.9, 119.0, 108.6, 103.0, 101.5, 93.6, 80.4, 58.3, 37.8, 29.8; MS (ES+) m/z 340.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700641B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-e9e53dec5d724fffb83242c3349b884c |
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| Source note | uspto-grants-2010_04 |
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