HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58817Generated: October 27, 2026
4-Methylmorpholine → HCID 130394597, compound
https://huagongshe.com/reaction/58817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 2-(4-Hydroxypiperidin-1-yl)acetic acid | HCID 11205927 | — |
| Reactant | (S)-benzyl 2-((S)-2-aminopropanamido)-3-(4-methoxyphenyl)propanoate | HCID 130394596 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 130394597 | HCID 130394597 | 87% |
Reaction Steps
To a solution of 2-(4-hydroxypiperidin-1-yl)acetic acid (0.41 g, 2.6 mmol) and (S)-benzyl 2-((S)-2-aminopropanamido)-3-(4-methoxyphenyl)propanoate (HCl salt, 0.93 g, 2.6 mmol) in dichloromethane (30 mL) at 0° C. was added HATU (1.1 g, 2.9 mmol) followed by N-methylmorpholine (1.05 g, 10.4 mmol). The reaction mixture was allowed to warm to ambient temperature and stirred for 1 h. Water (30 mL) was added and the resulting mixture was extracted with dichloromethane (30 mL×3). The organic extracts were combined, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/dichloromethane=5:1 to 1:1) to afford (S)-benzyl 2-((S)-2-(2-(4-hydroxypiperidin-1-yl)acetamido)propanamido)-3-(4-methoxyphenyl)propanoate (1.1 g, 87% yield) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09434761B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-bee3b889c20c4fd0926f4ca805d1d0a7 |
|---|
| Source note | uspto-grants-2016_09 |
|---|