Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481188Generated: October 27, 2026

Tert-butyl 1-(aminomethyl)cyclobutane-1-carboxylate → 1-{[(1-Cyano-4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carbonyl)-amino]-methyl}-cyclobutanecarboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1481188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 1-(aminomethyl)cyclobutane-1-carboxylateHCID 66797588—
Reactant1-Cyano-4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid methyl esterHCID 89812878—
SolventEthanolHCID 702—
Product1-{[(1-Cyano-4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carbonyl)-amino]-methyl}-cyclobutanecarboxylic acid tert-butyl esterHCID 8981304692.7%

Reaction Steps

A mixture of 1-cyano-4-hydroxy-7-phenylsulfanyl-isoquinoline-3-carboxylic acid methyl ester (43 mg) and 1-aminomethyl-cyclobutanecarboxylic acid tert-butyl ester (48 mg) in EtOH (0.5 mL) was microwaved at 140° C. for 1 h. The mixture was cooled, concentrated and the residue was column purified to give the desired product (58 mg). LC MS ESI+: 490 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409892B2
Source datasetuspto-grants-2016_08
ORD IDord-9eebe6de82bd4f8c8152a228a507b508
Source noteuspto-grants-2016_08