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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245405Generated: October 31, 2026

methyl 3-[5-(2-tert-butylsilyloxypropan-2-yl)-3-[4-[(2-methylquinolin-4-yl)methoxy]phenyl]-4H-1,2-oxazol-5-yl]prop-2-enoate → methyl 3-[5-(2-tert-butylsilyloxypropan-2-yl)-3-[4-[(2-methylquinolin-4-yl)methoxy]phenyl]-4H-1,2-oxazol-5-yl]propanoate

https://huagongshe.com/reaction/1245405

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 3-[5-(2-tert-butylsilyloxypropan-2-yl)-3-[4-[(2-methylquinolin-4-yl)methoxy]phenyl]-4H-1,2-oxazol-5-yl]prop-2-enoateHCID 131725998—
SolventMethanolHCID 887—
Productmethyl 3-[5-(2-tert-butylsilyloxypropan-2-yl)-3-[4-[(2-methylquinolin-4-yl)methoxy]phenyl]-4H-1,2-oxazol-5-yl]propanoateHCID 131725999—

Reaction Steps

The product from step 24d (0.24 g, 0.44 mmol) was dissolved in methanol (15 mL), degassed by bubbling nitrogen through the solution, charged with Rh/C and hydrogen gas (40 PSI), and shaken for 2 h. The reaction was filtered and concentrated to give 3-{5-(tert-butyl-dimethyl-silanyloxymethyl)-3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-propionic acid methyl ester as a crude oil. MS found: (M+H)+=549.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125870B2
Source datasetuspto-grants-2006_10
ORD IDord-66efaaec73ae4ee19f27db11eff66381
Source noteuspto-grants-2006_10