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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912125Generated: November 2, 2026

Boronic Acid → 2,6-difluoro-3-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-benzaldehyde

https://huagongshe.com/reaction/912125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoronic AcidHCID 61668—
Reactant2,4-Difluoro-3-formylphenylboronic acidHCID 3288955—
Reactant4-chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidineHCID 59244708—
Product2,6-difluoro-3-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-benzaldehydeHCID 86640119—

Reaction Steps

In the same manner as Example 1-B-10, using 4-chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine, and 2,4-difluoro-3-formylphenylboronic acid as a boronic acid, 2,6-difluoro-3-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-benzaldehyde was obtained. Methanol and sodium borohydride were added, which was stirred at room temperature for 1 hour, followed by elution with 2M ammonia methanol solution through SCX resin and then concentration. Purification by preparative TLC afforded the desired compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-0f21c22210c14fda9fb1127a206ba5ee
Source noteuspto-grants-2011_09