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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627140Generated: October 29, 2026

Cycloleucine → 1-((1-(tert-butoxycarbonyl)-3-(methoxycarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)methylamino)cyclopentanecarboxylic acid

https://huagongshe.com/reaction/1627140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloleucineHCID 2901—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-tert-Butyl 3-methyl 4-formyl-1H-pyrrolo[2,3-b]pyridine-1,3-dicarboxylateHCID 49761613—
SolventDichloromethaneHCID 6344—
Product1-((1-(tert-butoxycarbonyl)-3-(methoxycarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)methylamino)cyclopentanecarboxylic acidHCID 58293428—

Reaction Steps

To a 10 mL round bottom flask was added sodium triacetoxyborohydride (104 mg, 0.493 mmol) and 1-aminocyclopentanecarboxylic acid (42.4 mg, 0.329 mmol) in DCM (2 mL). The reaction mixture was stirred at room temperature for 30 min after which was added 1-tert-butyl 3-methyl 4-formyl-1H-pyrrolo[2,3-b]pyridine-1,3-dicarboxylate (50 mg, 0.164 mmol) in DCM (2 mL). The reaction was stirred at room temperature for 2 h and then quenched with MeOH (3 drops). The mixture was concentrated to afford the title compound, which was used in the next step without further purification. [M+H] calc'd for C21H27N3O6, 418; found, 418.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785429B2
Source datasetuspto-grants-2014_07
ORD IDord-948b940dd8124fd0b6c456f88d40482b
Source noteuspto-grants-2014_07