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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968196Generated: October 29, 2026

Sodium triacetoxyborohydride → HCID 58293470, compound

https://huagongshe.com/reaction/1968196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-tert-Butyl 3-methyl 4-formyl-1H-pyrrolo[2,3-b]pyridine-1,3-dicarboxylateHCID 49761613—
Reactant(2S)-2-Amino-1-(1-pyrrolidinyl)-1-butanoneHCID 58293418—
CatalystAcetic AcidHCID 176—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58293470HCID 5829347028.4%

Reaction Steps

A mixture of sodium triacetoxyborohydride (279 mg, 1.315 mmol) and (S)-2-amino-1-(pyrrolidin-1-yl)butan-1-one (123 mg, 0.789 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 (200 mg, 0.657 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 (83mg, 28.4%). [M+H] calc'd for C23H32N4O5, 445; found, 445.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420816B2
Source datasetuspto-grants-2013_04
ORD IDord-14b6d4dbaa0e4296b21a455eea752414
Source noteuspto-grants-2013_04