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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952059Generated: November 3, 2026

Sodium borohydride → HCID 59593284, compound

https://huagongshe.com/reaction/1952059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59593312HCID 59593312—
SolventMethanolHCID 887—
ProductHCID 59593284HCID 59593284—

Reaction Conditions

Temperature50 °C

Reaction Steps

To [2-Chloro-6-(4-chloro-benzylamino)-pyridin-3-yl]-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone (P-0048, 0.045 g, 0.00011 mol, prepared as described in Example 27) was added methanol (10 mL) and sodium borohydride (0.00428 g, 0.000113 mol). The reaction was allowed to stir at 50° C. overnight. The volatiles were removed from the reaction, and the resulting material was extracted with ethyl acetate and 1M aqueous sodium bicarbonate. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with dichloromethane followed by 1% methanol in dichloromethane to give the compound (P-0050, 31 mg, 68%). MS (ESI) [M+H+]+=399.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404700B2
Source datasetuspto-grants-2013_03
ORD IDord-67723ecbfc724963ac35c34417a6bbd5
Source noteuspto-grants-2013_03