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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445132Generated: November 3, 2026

2-(6-Chloro-3-nitropyridin-2-yl)-1,2,3,4-tetrahydroisoquinoline → 2-(5-chloro-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydro-isoquinoline

https://huagongshe.com/reaction/1445132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(6-Chloro-3-nitropyridin-2-yl)-1,2,3,4-tetrahydroisoquinolineHCID 43152677—
ReactantHCID 178456138HCID 178456138—
Product2-(5-chloro-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydro-isoquinolineHCID 86615276—

Reaction Steps

In accordance with the same procedures as in Step 3 of Example 642, except for using 2-(6-chloro-3-nitropyridin-2-yl)-1,2,3,4-tetrahydroisoquinoline prepared in Preparation 7 and isopropenylmagnesium bromide, the titled compound was obtained as yellow oil. (Yield: 35%) The product was used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662832B2
Source datasetuspto-grants-2010_02
ORD IDord-54bb5fa3e7994a6bb1a1c501b8984102
Source noteuspto-grants-2010_02