HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570893Generated: October 30, 2026
Diisopropylethylamine → HCID 71293422, compound
https://huagongshe.com/reaction/570893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| 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 | HCID 71293493 | HCID 71293493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71293422 | HCID 71293422 | 29.9% |
Reaction Steps
Intermediate 26 (250 mg, 0.46 mmol) was dissolved in DMF (5 mL), and then diisopropylethylamine (240 μL, 1.4 mmol) and HATU (266 mg, 0.7 mmol) were added. The reaction mixture was stirred at RT for 40 minutes, then N,N,N-trimethylpentanediamine (288 mg, 2.0 mmol) in DMF (1 mL) was added, and stirring was continued for a further 18 hours. The reaction mixture was partitioned between EtOAc and water. The organic layer was separated, and the aqueous layer extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and evaporated in vacuo. The resulting residue was purified by silica gel chromatography eluting with a gradient of 4-8% (2 M NH3 in MeOH) in DCM followed by a gradient of 6-7% (2 M NH3 in MeOH) in DCM. The resulting residue was purified by MDAP to yield the title compound as an off-white solid (88 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09023855B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-56e930b0d38e4f198d065abfd027c611 |
|---|
| Source note | uspto-grants-2015_05 |
|---|