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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071346Generated: October 27, 2026

Diisopropylethylamine → N-(1-tert-Butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-benzyloxycarbonyl-4-piperidinecarboxamide

https://huagongshe.com/reaction/1071346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
ReactantHCID 22393192HCID 22393192—
SolventAcetonitrileHCID 6342—
ProductN-(1-tert-Butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-benzyloxycarbonyl-4-piperidinecarboxamideHCID 22393147102.4%

Reaction Steps

N-Benzyloxycarbonylisonipecotyl chloride (5 g) was added to a solution of 4-amino-1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridine (3 g) and diisopropylethyamine (2.16 g) in acetonitrile (40 ml) and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into ice-water and extracted with chloroform. The residue obtained by water washing, drying and then concentration under reduced pressure was purified by silica gel column chromatography to give 6.3 g of N-(1-tert-butoxycarbonyl-1H-pyrrolo-[2,3-b]pyridin-4-yl)-1-benzyloxycarbonyl-4-piperidinecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906061B2
Source datasetuspto-grants-2005_06
ORD IDord-5cd7f1c4295b4f2d82ee403ff77ec675
Source noteuspto-grants-2005_06