HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930294Generated: October 28, 2026
Ammonia → N-(3-((4SR,6SR)-2-amino-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4-fluorophenyl)-5-chloro-3-methyl-2-pyridinecarboxamide
https://huagongshe.com/reaction/930294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-(3-((4S,6S)-2-benzamido-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4-fluorophenyl)-5-chloro-3-methylpicolinamide | HCID 86732125 | — |
| Product | N-(3-((4SR,6SR)-2-amino-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4-fluorophenyl)-5-chloro-3-methyl-2-pyridinecarboxamide | HCID 86732126 | 51.3% |
Reaction Steps
A sealable vial was charged with N-(3-((4S,6S)-2-benzamido-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4-fluorophenyl)-5-chloro-3-methylpicolinamide (rac 4n, 0.050 g, 0.091 mmol) and ammonia (2.0M solution in methanol; 3.0 ml, 6.00 mmol). The reaction mixture was heated to 80° C. for 17 hs. The reaction mixture was concentrated an the residue was diluted with a minimal amount of CH2Cl2. Purification by silica gel chromatography (gradient 0.0 to 5.0% 2 M ammonia in MeOH/CH2Cl2) afforded the title compound (0.0104 g, 0.023 mmol, 51.3% yield) as a white solid. MS m/z=445.0 [M+H]+. Calculated for C19H17ClF4N4O2: 444.098.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09296734B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-3d69734dc13e4459bf0e39741f4f2ea3 |
|---|
| Source note | uspto-grants-2016_03 |
|---|