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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097503Generated: October 31, 2026

Methylboronic Acid → 5-Benzyloxymethyl-3-methyl-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one

https://huagongshe.com/reaction/2097503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylboronic AcidHCID 139377—
Reactant3-Bromo-1,5-bis(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 66602503—
Reactant5-Benzyloxymethyl-3-bromo-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 66602856—
Product5-Benzyloxymethyl-3-methyl-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 6660285096%

Reaction Steps

Reaction and post treatment were carried out in the same manner as in Reference example 20-(b) except for using 30.8 g (66.3 mmol) of 5-benzyloxymethyl-3-bromo-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Reference example 24-(b) in place of 3-bromo-1,5-bis(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one, and using 12.0 g (200 mmol) of methylboronic acid in place of propylboronic acid, respectively, whereby 25.3 g of the title compound was obtained as a brownish oil. (Yield: 96%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-b0e63192eb424a12b77b74e1c801d405
Source noteuspto-grants-2013_05