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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590831Generated: October 30, 2026

Sodium borohydride → (6-chloro-3-morpholino-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methanol

https://huagongshe.com/reaction/590831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-chloro-3-morpholino-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehydeHCID 118272219—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(6-chloro-3-morpholino-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methanolHCID 118271519—

Reaction Steps

6-Chloro-3-morpholino-1-trityl-1H-pyrazolo [4,3-c]pyridine-4-carbaldehyde (292.2 mg, 0.574 mmol) was dissolved in DCM (3 mL) and methanol (3 mL). Sodium borohydride (21.72 mg, 0.574 mmol) was then added and the reaction mixture was stirred at rt for 15 min. The reaction was quenched with water and extracted with DCM. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo while loading onto silica gel. Purification by flash chromatography (5-40% EtOAc/Hexanes) gave (6-chloro-3-morpholino-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methanol. MS ESI calc'd. For C30H28ClN4O2 [M+H]+ 511. found 511.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-5c51c03f63804ec1be8f4d45309bd289
Source noteuspto-grants-2016_01