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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473197Generated: October 26, 2026

1-(2-Bromoethyl)piperidine → 2-Tert-butoxy-2-[4-(4-chlorophenyl)-6-methyl-7-oxo-1-[2-(1-piperidyl)ethyl]pyrrolo[2,3-c]pyridin-5-yl]acetic acid

https://huagongshe.com/reaction/1473197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Bromoethyl)piperidineHCID 426611—
Reactantmethyl 2-(tert-butoxy)-2-(4-(4-chlorophenyl)-6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-5-yl)acetateHCID 89463134—
Product2-Tert-butoxy-2-[4-(4-chlorophenyl)-6-methyl-7-oxo-1-[2-(1-piperidyl)ethyl]pyrrolo[2,3-c]pyridin-5-yl]acetic acidHCID 71538756—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 2 from methyl 2-(tert-butoxy)-2-(4-(4-chlorophenyl)-6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-5-yl)acetate and 1-(2-bromoethyl)piperidine. 1H NMR (400 MHz, METHANOL-d4) ppm 7.62-7.52 (m, 3H), 7.48-7.41 (m, 1H), 7.39-7.31 (m, 1H), 6.09-6.03 (m, 1H), 5.27 (s, 1H), 5.00-4.91 (m, 2H), 3.75 (s, 3H), 3.68-3.53 (m, 4H), 3.12-2.95 (m, 2H), 2.04-1.92 (m, 2H), 1.92-1.75 (m, 2H), 1.62-1.46 (m, 2H), 0.96 (s, 9H); LCMS (m/z) ES+=500 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012642B2
Source datasetuspto-grants-2015_04
ORD IDord-8c98092c59744b4b859db1fb96f3e601
Source noteuspto-grants-2015_04