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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968210Generated: October 29, 2026

Sodium triacetoxyborohydride → HCID 58293496, compound

https://huagongshe.com/reaction/1968210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 28204508HCID 28204508—
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 58293496HCID 5829349690.3%

Reaction Steps

A mixture of sodium triacetoxyborohydride (104 mg, 0.493 mmol) and (R)-2-amino-N-cyclopentyl-3-methylbutanamide (68.1 mg, 0.370 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 (75 mg, 0.246 mmol) in DCE (2 mL) was added, followed by acetic acid (1 drop). The reaction mixture 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 (105 mg, 90%). [M+H] calc'd for C25H36N4O5, 473; found, 473.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420816B2
Source datasetuspto-grants-2013_04
ORD IDord-e61f47979cef46c68ab4bc33e6ae9405
Source noteuspto-grants-2013_04