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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425645Generated: October 30, 2026

Dibenzofuran-4-boronic acid → HCID 59263453, compound

https://huagongshe.com/reaction/425645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzofuran-4-boronic acidHCID 2734328—
Reactant6-(Dimethylamino)pyridine-3-boronic acidHCID 2763271—
Reactant4'-bromo-1'-pentylspiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1'H)oneHCID 59263339—
Reactant4'-bromospiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1H)-oneHCID 59263372—
ProductHCID 59263453HCID 59263453—

Reaction Steps

Following the procedure as described in EXAMPLE 4, and making non-critical variations using 4′-bromospiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-2′(1′H)-one to replace 4′-bromo-1′-pentylspiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-2′(1′H)-one, and dibenzo[b,d]furan-4-ylboronic acid to replace [6-(dimethylamino)pyridin-3-yl]boronic acid, the title compound was obtained (10%) as a colorless solid: mp>230° C.; 1H NMR (300 MHz, DMSO-d6) δ 10.77 (s, 1H), 8.04 (d, 1H), 7.97 (dd, 1H), 7.43-7.42 (m, 3H), 7.34-7.29 (m, 3H), 7.16 (t, 1H), 6.98 (d, 1H), 6.89 (d, 1H), 6.25 (s, 1H), 5.69 (d, 2H), 4.41 (ABq, 2H); MS (ES+) m/z 448.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106087B2
Source datasetuspto-grants-2012_01
ORD IDord-966cb28579064c99bfd6aaa4dd8fd168
Source noteuspto-grants-2012_01