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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968185Generated: October 30, 2026

tert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylate → HCID 67225102, compound

https://huagongshe.com/reaction/1968185

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylateHCID 2756485—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-tert-Butyl 4-methyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1,4-dicarboxylateHCID 58293521—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 67225102HCID 6722510285.3%

Reaction Steps

To a solution of 1-tert-butyl 4-methyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1,4-dicarboxylate (91 mg, 0.3 mmol) in MeOH (2 mL) was added AcOH (5 drops) and tert-butyl 3-(aminomethyl)pyrrolidine-1-carboxylate (90 mg, 0.45 mmol). After stirring for 60 min at rt, the reaction mixture was cooled to 0° C. Sodium cyanoborohydride (57 mg, 0.9 mmol) was added, and the reaction mixture was stirred for an additional 3 h at rt. The mixture was quenched with water and extracted with ethyl acetate. The combined organic layers washed with saturated NaHCO3 and with brine, dried over Na2SO4, and concentrated in vacuo to give 125 mg of crude 1-tert-butyl 4-methyl 3-(((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methylamino)methyl)-1H-pyrrolo[2,3-b]pyridine-1,4-dicarboxylate as a colorless oil which was used without further purification. [M+H] found 489.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420816B2
Source datasetuspto-grants-2013_04
ORD IDord-7ea7d19a6d74425eaf0c4b9254ca8e7f
Source noteuspto-grants-2013_04