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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692887Generated: October 31, 2026

HCID 67279564, compound → HCID 59603444, compound

https://huagongshe.com/reaction/1692887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67279564HCID 67279564—
ReactantHCID 67280787HCID 67280787—
ProductHCID 59603444HCID 59603444—

Reaction Steps

Following the procedures to prepare 104, racemic cis-3-fluoro-N,N-dimethylpiperidin-4-amine was converted to 1-((2-(1H-indol-3-yl)-9-methyl-6-morpholino-9H-purin-8-yl)methyl)-3-fluoro-N,N-dimethylpiperidin-4-amine. The enantiomers of the final product were separated by SFC to give 123. LCMS: M+H+=493.2. 1H-NMR (400 MHz, DMSO-d6): δ 11.5 (s, 1H), 8.61 (m, 1H), 8.13 (m, 1H), 7.42 (m, 1H), 7.14 (m, 2H), 4.27 (s, br, 4H), 3.85 (s, 3H), 3.79 (m, 6H), 3.04 (m, 1H), 2.91 (m, 1H), 2.05-2.29 (m, 5H), 1.59-1.84 (m, 2H), 1.17 (t, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158625B2
Source datasetuspto-grants-2012_04
ORD IDord-26fc67093b054e66a7c411bb181b5601
Source noteuspto-grants-2012_04