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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965705Generated: October 30, 2026

HCID 72268644, compound → HCID 59352304, compound

https://huagongshe.com/reaction/1965705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 72268644HCID 72268644—
ReactantHCID 76748362HCID 76748362—
ProductHCID 59352304HCID 59352304—

Reaction Steps

Following the procedure as described in EXAMPLE 11.27 and making non-critical variations using N′-hydroxy-3-[(2′-oxo-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-1′(2′H)-yl)methyl]benzenecarboximidamide to replace N′-hydroxy-3-[(2′-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-1′(2′H)-yl)methyl]benzenecarboximidamide, 1′-[3-(5-methyl-1,2,4-oxadiazol-3-yl)benzyl]-2,3-dihydrospiro[furo[2,3-g][1,4]benzodioxine-8,3′-indol]-2′(1′H)-one was obtained (65%) as a colorless solid: mp 90-95° C. (ethyl acetate/diethyl ether); 1H NMR (300 MHz, CDCl3) δ 7.89-7.87 (m, 2H), 7.58-7.53 (m, 2H), 7.25-7.15 (m, 2H), 7.03-6.95 (m, 2H), 6.50 (s, 1H), 6.20 (s, 1H), 5.15-4.64 (m, 4H), 4.16-4.07 (m, 4H), 2.62 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 178.1, 177.3, 167.8, 155.2, 144.7, 142.4, 138.4, 137.9, 132.2, 130.8, 130.2, 129.3, 127.2, 126.3, 125.5, 124.2, 123.7, 121.5, 111.6, 109.9, 99.3, 80.0, 64.7, 64.0, 57.8, 43.1, 12.4; MS (ES+) m/z 467.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-c344c4964d39475eb512b3acbb6fc3ba
Source noteuspto-grants-2013_04