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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473200Generated: November 1, 2026

2-Chloromethyl-imidazo(1,2-A)pyridine → HCID 71538214, compound

https://huagongshe.com/reaction/1473200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloromethyl-imidazo(1,2-A)pyridineHCID 957614—
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—
ProductHCID 71538214HCID 71538214—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 2 using 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 2-(chloromethyl)imidazo[1,2-a]pyridine. 1H NMR (400 MHz, CHLOROFORM-d) ppm 8.33-8.40 (m, 1H) 8.18-8.25 (m, 1H) 8.10-8.17 (m, 1H) 7.70-7.79 (m, 1H) 7.59-7.65 (m, 1H) 7.51-7.56 (m, 1H) 7.44-7.50 (m, 2H) 7.34-7.41 (m, 1H) 7.29-7.34 (m, 1H) 6.18-6.25 (m, 1H) 6.00-6.05 (m, 1H) 5.88-5.98 (m, 1H) 5.35 (s, 1H) 3.67 (s, 3H) 1.02 (s, 9H); LCMS (m/z) ES+=519 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012642B2
Source datasetuspto-grants-2015_04
ORD IDord-182ce6d297db420e82ec7af8eb6546c2
Source noteuspto-grants-2015_04