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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203451Generated: November 2, 2026

[2-(Benzyloxy)-5-methylphenyl]boronic acid → HCID 89544105, compound

https://huagongshe.com/reaction/2203451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(Benzyloxy)-5-methylphenyl]boronic acidHCID 14631588—
Reactant(5-Chloro-2-hydroxyphenyl)boronic Acid (contains varying amounts of Anhydride)HCID 23005362—
Reactant5-bromo-7-(4-methoxybenzyl)imidazo[1,5-a]pyrazin-8(7H)-oneHCID 89544047—
ReactantHCID 89544282HCID 89544282—
ProductHCID 89544105HCID 89544105—

Reaction Steps

Following the procedure as described in EXAMPLE 4 and making non-critical variations to replace 5-bromo-7-(4-methoxybenzyl)imidazol[1,5-a]pyrazin-8(7H)-one with 3-benzhydryl-5-bromobenzo[d]oxazol-2(3H)-one and (5-chloro-2-hydroxyphenyl)boronic acid with (2-(benzyloxy)-5-methylphenyl)boronic acid, 3-benzhydryl-5-(2-(benzyloxy)-5-methylphenyl)benzo[d]oxazol-2(3H)-one was obtained as a colorless solid in quantitative yield (1.05 g): 1H NMR (300 MHz, CDCl3) δ7.30-7.16 (m, 17H), 6.98 (dd, J=8.3, 1.7 Hz, 1H), 6.80-6.76 (m, 3H), 6.68 (s, 1H), 4.95 (s, 2H), 2.24 (s, 3H); MS (ES+) m/z 497.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365578B2
Source datasetuspto-grants-2016_06
ORD IDord-01a8611199ab4a46a8d8c092dbc35830
Source noteuspto-grants-2016_06