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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506822Generated: November 3, 2026

1-Boc-4-(aminomethyl)piperidine → HCID 68468951, compound

https://huagongshe.com/reaction/506822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
ReactantHCID 68467994HCID 68467994—
ProductHCID 68468951HCID 6846895148.7%

Reaction Steps

The product is prepared by following the procedure described in example 52c, starting with 0.3 g of 3-[4-chloromethyl-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-5,6-dimethoxy-1-methyl-1H-pyrrolo[3,2-b]pyridine and 0.315 g of 4-(aminomethyl)-1-N-Boc-piperidine instead of the N-Boc-ethylenediamine used in example 52c. 0.197 g of tert-butyl 4-({[2-(5,6-dimethoxy-1-methyl-1H-pyrrolo[3,2-b]pyridin-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-4-ylmethyl]amino}methyl)piperidine-1-carboxylate is obtained with the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786114B2
Source datasetuspto-grants-2010_08
ORD IDord-dfa0d71af18b40f48c4b49610176ea65
Source noteuspto-grants-2010_08