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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490530Generated: October 31, 2026

3-Aminoazetidine, 3-BOC protected → HCID 67147746, compound

https://huagongshe.com/reaction/490530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminoazetidine, 3-BOC protectedHCID 1519405—
ReactantHCID 67147535HCID 67147535—
ProductHCID 67147714HCID 67147714—
ProductHCID 67147746HCID 67147746200.1%

Reaction Steps

{1-[2-(5,6-Dimethoxy-1-methyl-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyrid-4-ylmethyl]azetidin-3-yl}carbamic acid tert-butyl ester is prepared as described in Example 200b starting with 0.14 g of 4-chloromethyl-2-(5,6-dimethoxy-1-methyl-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine and 0.118 g of azetidin-3-ylcarbamic acid tert-butyl ester instead of the piperid-4-ol used in Example 200b. After purification by flash-pack chromatography (SiO2, dichloromethane/methanol 95/5 by volume as eluent), 0.135 g of {1-[2-(5,6-dimethoxy-1-methyl-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyrid-4-ylmethyl]azetidin-3-yl}carbamic acid tert-butyl ester is obtained, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528147B2
Source datasetuspto-grants-2009_05
ORD IDord-aa3260f019a0470b81128ff27bea7118
Source noteuspto-grants-2009_05