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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945724Generated: November 2, 2026

4-Bromo-1H-pyrrolo(3,2-c)pyridine → 4-(1-((9-methyl-6-morpholino-2-(1H-pyrrolo[3,2-c]pyridin-4-yl)-9H-purin-8-yl)methyl)piperidin-4-yl)morpholine

https://huagongshe.com/reaction/1945724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1H-pyrrolo(3,2-c)pyridineHCID 24729217—
Reactant4-(1-((9-methyl-6-morpholino-2-(tributylstannyl)-9H-purin-8-yl)methyl)piperidin-4-yl)morpholineHCID 59606164—
Product4-(1-((9-methyl-6-morpholino-2-(1H-pyrrolo[3,2-c]pyridin-4-yl)-9H-purin-8-yl)methyl)piperidin-4-yl)morpholineHCID 59605820—

Reaction Steps

Following the procedures to prepare 124, 4-(1-((9-Methyl-6-morpholino-2-(tributylstannyl)-9H-purin-8-yl)methyl)piperidin-4-yl)morpholine and 4-bromo-1H-pyrrolo[3,2-c]pyridine were reacted to give 133. LCMS: M+H+=518.3. 1H-NMR (400 MHz, DMSO-d6): δ 11.55 (s, 1H), 8.30 (d, 1H), 7.51 (d, 1H), 7.48 (d, 1H), 7.20 (d, 1H), 4.30 (m, 4H), 3.80 (s, 3H), 3.78 (m, 6H), 3.55 (m, 4H), 2.88 (m, 2H), 2.44 (m, 4H), 2.09 (m, 2H), 1.77 (m, 2H), 1.40 (m, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-f30b72109b834e4aa12828674f2c787d
Source noteuspto-grants-2013_03