HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777935Generated: October 25, 2026
Triethylamine → Racemic 6-amino-4-(2-((dimethylamino)methyl)morpholino)nicotinonitrile
https://huagongshe.com/reaction/1777935
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethyl-morpholin-2-ylmethyl-amine | HCID 3401489 | — |
| Reactant | 6-Amino-4-fluoronicotinonitrile | HCID 118036901 | — |
| Product | Racemic 6-amino-4-(2-((dimethylamino)methyl)morpholino)nicotinonitrile | HCID 118036458 | — |
Reaction Steps
A mixture of racemic 2-dimethylaminomethylmorpholine (670 mg, 4.65 mmol), 6-amino-4-fluoronicotinonitrile (intermediate 21, 637 mg, 4.65 mmol) and triethylamine (2.59 ml, 18.6 mmol) was heated at 60° C. in a septum sealed reaction vessel under argon for 10 h. The reaction mixture was evaporated, partitioned between aq. hydrochloric acid (2 M) and DCM (2×), the aqueous layer basified with aqueous NaHCO3, extracted a further 10× with DCM containing 10% MeOH, the combined DCM layers from the basic extraction, dried over Na2SO4 and evaporated. The residue was applied to a 24 g RediSep® silica column as a DCM solution and purified by normal phase chromatography, eluting with a gradient from DCM to 20% MeOH in DCM. Product containing fractions were combined and evaporated to give the title compound as a beige foam. (UPLC-MS 6) tR 0.28; ESI-MS 262.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09266883B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-abe6c3756c9e4f3ab951daf097a042b3 |
|---|
| Source note | uspto-grants-2016_02 |
|---|