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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355878Generated: October 30, 2026

HCID 58864274, compound → HCID 178432157, compound

https://huagongshe.com/reaction/2355878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58864274HCID 58864274—
Reactant(R)-3-[2-Methyl-1-(2-trimethylsilanyl-ethanesulfonyl)-1H-benzoimidazol-5-yl]-2-{[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carbonyl]-amino}-propionic acid methyl esterHCID 58864319—
ReactantHCID 58864337HCID 58864337—
ReactantHCID 68706663HCID 68706663—
ProductHCID 178432157HCID 178432157—

Reaction Steps

The 1:1 mixture of (R)-3-[2-Methyl-1-(2-trimethylsilanyl-ethanesulfonyl)-1H-benzoimidazol-5-yl]-2-{[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carbonyl]-amino}-propionic acid methyl ester and (R)-3-[2-Methyl-3-(2-trimethylsilanyl-ethanesulfonyl)-3H-benzoimidazol-5-yl]-2-{[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carbonyl]-amino}-propionic acid methyl ester was treated as described above for (R)-2-{[4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carbonyl]-amino}-3-[1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indazol-5-yl]-propionic acid. The hydrolysis conditions (lithium hydroxide/methanol-tetrahydrofuran-water (1:1:1) at −15° C. overnight were used. The title compound was obtained as a white solid (25%). Mass spec.: 477.24 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754732B2
Source datasetuspto-grants-2010_07
ORD IDord-adf5a740ca414ce793594c00f57f48e1
Source noteuspto-grants-2010_07