HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953921Generated: October 30, 2026
Diisopropylethylamine → HCID 54347045, compound
https://huagongshe.com/reaction/1953921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 23297590 | HCID 23297590 | — |
| Reactant | HCID 54010435 | HCID 54010435 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54347045 | HCID 54347045 | 51.3% |
Reaction Steps
To a solution of (S)-2-[(4-dimethylamino-benzyl)-methyl-amino]-4-methyl-pentanoic acid (0.28 g, 1.01 mmol) in 15 mL of DMF was added HBTU (0.38 g, 1.01 mmol) and diisopropylethylamine (0.65 g, 5.05 mmol). The mixture was stirred for 30 minutes at 0° C. A solution of 2-amino-3-(4-benzyloxyphenyl)-N-(1-propyl-piperidin-3-yl)propionamide (0.40 g, 1.01 mmol) in 15 mL of DMF was added to the reaction mixture. The reaction mixture was allowed to reach the room temperature and was stirred for another 30 minutes. The mixture was diluted with 40 mL of ethyl acetate, washed with 1N HCl (2×10 mL), saturated NaHCO3 (2×10 mL) and saturated solution of brine (2×10 mL). The organic layer was separated, dried with Na2SO4 and evaporated to dryness. The crude residue was purified by chromatography (silica gel, 6:4 hexane/ethyl acetate). The purified product was crystallized from methylene chloride and petroleum ether to give the title compound (0.34 g, 49%) as a white powder; mp 131-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06117841 |
|---|
| Source dataset | uspto-grants-2000_09 |
|---|
| ORD ID | ord-5a675aa97ad44bd3a3a71044da17db08 |
|---|
| Source note | uspto-grants-2000_09 |
|---|