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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968813Generated: October 29, 2026

Methanol → HCID 58625122, compound

https://huagongshe.com/reaction/1968813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,4,6-TrimethylbenzaldehydeHCID 10254—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58625068HCID 58625068—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58625122HCID 58625122—

Reaction Steps

2,4,6-Trimethyl-benzaldehyde (0.0005 mol) was added to a mixture of [6-(3-amino-phenoxy)-3-propyl-3,4-dihydro-quinazolin-2-yl]-carbamic acid tert-butyl ester (0.0005 mol) in DCE (3 mL) and the mixture was stirred for 5 min. at room temperature, and then NaBH(OAc)3 (0.0006 mol) was added and the reaction mixture was stirred overnight at room temperature. The excess NaBH(OAc)3 was decomposed with CH3OH, and the solvent was evaporated. The obtained residue was purified by Biotage column chromatography (eluent: 100% CH2Cl2). The purest product fractions were collected and then the solvent was evaporated and co-evaporated with toluene to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426429B2
Source datasetuspto-grants-2013_04
ORD IDord-73b5701218954d34a55c6e2294e2e8c0
Source noteuspto-grants-2013_04