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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627093Generated: November 1, 2026

1-BOC-3-Aminopiperidine → HCID 67224484, compound

https://huagongshe.com/reaction/1627093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BOC-3-AminopiperidineHCID 545809—
ReactantSodium cyanoborohydride [MI]HCID 20587905—
Reactant1-tert-Butyl 4-methyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1,4-dicarboxylateHCID 58293521—
SolventAcetic acid methanolHCID 10129899—
ProductHCID 67224484HCID 6722448479%

Reaction Steps

To a solution of 1-tert-butyl 4-methyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1,4-dicarboxylate (304 mg, 1.00 mmol) in 9:1 MeOH-Acetic Acid (2 mL) at 0° C. was added tert-butyl 3-aminopiperidine-1-carboxylate (300 mg, 1.50 mmol) and the reaction mixture was stirred at rt for 1 h. Sodium cyanotrihydroborate (314 mg, 5.00 mmol) was added slowly portion wise and the reaction mixture was stirred at rt over night, quenched with water, and extracted with ethyl acetate. The combined organic layers were washed with saturated NaHCO3 and with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by silica gel chromatography (30% to 70% Hexane-EtOAc) to give 307 mg of methyl 3-((1-(tert-butoxycarbonyl) piperidin-3-ylamino)methyl)-1H-pyrrolo[2,3-b]pyridine-4-carboxylate as a colorless oil. [M+H] found 389.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785429B2
Source datasetuspto-grants-2014_07
ORD IDord-5d7c0026b6694817873a6d2155920c5b
Source noteuspto-grants-2014_07