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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708484Generated: October 30, 2026

Ethyl 2-[2-butyl-3,4-dihydro-4-oxo-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-6-quinazolinyl]hexahydro-pyrrolo[1,2-b]isoxazole-3-carboxylate → HCID 178441448, compound

https://huagongshe.com/reaction/1708484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-[2-butyl-3,4-dihydro-4-oxo-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-6-quinazolinyl]hexahydro-pyrrolo[1,2-b]isoxazole-3-carboxylateHCID 18958919—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 178441448HCID 17844144850.4%

Reaction Steps

A solution of 0.174 g of ethyl 2-[2-butyl-3,4-dihydro-4-oxo-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-6-quinazolinyl]hexahydro-pyrrolo[1,2-b]isoxazole-3-carboxylate in 2.0 ml of ethanol and 1.0 ml of chloroform containing 2.0 ml of 3M HC1 in ethyl acetate is stirred at room temperature for 1 hour. The volatiles are evaporated in vacuo to a residue which is purified by column chromatography on silica gel by elution with 9:1 chloroform-methanol to give 0.063 g of the desired product as a solid. FAB Mass spec 620 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05358951
Source datasetuspto-grants-1994_10
ORD IDord-2b4ac4ee69cf4cd2beea0855b7345ff0
Source noteuspto-grants-1994_10