HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67279564, compound → HCID 59603444, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67279564 | HCID 67279564 | — |
| Reactant | HCID 67280787 | HCID 67280787 | — |
| Product | HCID 59603444 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158625B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-26fc67093b054e66a7c411bb181b5601 |
| Source note | uspto-grants-2012_04 |