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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965682Generated: October 30, 2026

HCID 75110103, compound → HCID 59352754, compound

https://huagongshe.com/reaction/1965682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 75110103HCID 75110103—
SolventPyridineHCID 1049—
ProductHCID 59352754HCID 59352754158.1%

Reaction Steps

A stirred solution of 2-(4′-chloro-2′-oxospiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-1′(2′H)-yl)-N′-[(cyclopropylcarbonyl)oxy]ethanimidamide (0.24 g, 0.52 mmol) in pyridine (1 mL) was heated at 170° C. for 30 min in a microwave reactor. The solution was concentrated in vacuo to dryness, purified by flash chromatography with ethyl acetate in hexanes (15% to 50% gradient) to afford 4′-chloro-1′-[(5-cyclopropyl-1,2,4-oxadiazol-3-yl)methyl]spiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-2′(1′H)-one (0.36 g, 16%) as a colorless solid: mp 180-182° C.; 1H NMR (300 MHz, CDCl3) δ7.19 (dd, J=8.1, 8.1 Hz, 1H), 6.99 (d, J=8.4 Hz, 1H), 6.77 (d, J=7.8 Hz, 1H), 6.46 (s, 1H), 6.28 (s, 1H), 5.86 (d, J=1.2 Hz, 1H), 5.04 (ABq, 2H), 4.94 (ABq, 2H), 2.20-2.10 (m, 1H). 1.26-1.12 (m, 4H); 13C NMR (75 MHz, CDCl3) δ182.9, 177.0, 165.4, 156.8, 149.2, 143.0, 142.1, 131.6, 130.0, 128.4, 124.6, 116.5, 107.4, 103.0, 101.5, 93.2, 58.7, 36.1, 10.57, 10.53, 7.8; MS (ES+) m/z 438.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-04ea8456f5dc44dfa0dbb5a52c0d2f25
Source noteuspto-grants-2013_04