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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626806Generated: November 3, 2026

Ethyl 2-(4-bromobenzyl)benzoate → Ethyl 2-{4-[4-({5-(benzyloxy)-4-[(2-tert-butoxy-2-oxoethyl)carbamoyl]-6-methylpyrimidin-2-yl}methyl)piperidin-1-yl]benzyl}benzoate

https://huagongshe.com/reaction/1626806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(4-bromobenzyl)benzoateHCID 68193210—
ReactantTert-butyl ({[5-(benzyloxy)-6-methyl-2-(piperidin-4-ylmethyl)pyrimidin-4-yl]carbonyl}amino)acetate hydrochlorideHCID 86670085—
ProductEthyl 2-{4-[4-({5-(benzyloxy)-4-[(2-tert-butoxy-2-oxoethyl)carbamoyl]-6-methylpyrimidin-2-yl}methyl)piperidin-1-yl]benzyl}benzoateHCID 6819325772%

Reaction Steps

In accordance with Example 1-(9), but using tert-butyl ({[5-(benzyloxy)-6-methyl-2-(piperidin-4-ylmethyl)pyrimidin-4-yl]carbonyl}amino)acetate hydrochloride instead of tert-butyl 5-(benzyloxy)-6-methyl-2-(piperidin-4-ylmethyl)pyrimidine-4-carboxylate hydrochloride, and ethyl 2-(4-bromobenzyl)benzoate instead of [(4′-bromobiphenyl-4-yl)methoxy](tert-butyl)dimethylsilane, the title compound (yield 72%) was afforded as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785462B2
Source datasetuspto-grants-2014_07
ORD IDord-874e7e09a35240f89f2919ade0d19d86
Source noteuspto-grants-2014_07