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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627111Generated: November 1, 2026

Sodium triacetoxyborohydride → HCID 58293435, compound

https://huagongshe.com/reaction/1627111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 28197509HCID 28197509—
Reactant1-tert-Butyl 3-methyl 4-formyl-1H-pyrrolo[2,3-b]pyridine-1,3-dicarboxylateHCID 49761613—
CatalystAcetic AcidHCID 176—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58293435HCID 58293435102.9%

Reaction Steps

A mixture of sodium triacetoxyborohydride (139 mg, 0.657 mmol) and (R)-2-amino-4-methyl-1-(pyrrolidin-1-yl)pentan-1-one (91 mg, 0.493 mmol) in DCE (2 mL) was stirred at room temperature for 30 min. The reaction mixture was cooled to 0° C. A solution of 1-tert-butyl 3-methyl 4-formyl-1H-pyrrolo[2,3-b]pyridine-1,3-dicarboxylate (100 mg, 0.329 mmol) in DCE (2 mL) was added, followed by acetic acid (1 drop). The reaction was stirred at 0° C. for 30 min and then at room temperature for 3 h. Purification by silica column chromatography (EtOAc/DCM, 0-10%) afforded the title compound as a yellow oil (160 mg, 93%). [M+H] calc'd for C25H36N4O5, 473; found, 473.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785429B2
Source datasetuspto-grants-2014_07
ORD IDord-4df58934f0e74cb5a4688329ab850dcf
Source noteuspto-grants-2014_07