HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57718Generated: October 28, 2026
Diisopropylethylamine → HCID 89722227, compound
https://huagongshe.com/reaction/57718
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 | Methyl 1-amino-1H-imidazole-5-carboxylate | HCID 11665425 | — |
| Reactant | 1-Benzyl-4-(trifluoromethyl)pyrrolidine-3-carboxylic acid | HCID 19691386 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89722227 | HCID 89722227 | 85.9% |
Reaction Steps
To a solution of compound 2 (2.0 g, 14.1 mmol), 1-Benzyl-4-trifluoromethyl-pyrrolidine-3-carboxylic acid (4.06 g, 14.9 mmol) and DIEA (10 mL, 42.5 mmol) in DMF (30 mL) was added HATU (8.1 g, 21.2 mmol). The resulting reaction mixture was stirred at r.t. overnight. The reaction was monitored by LC-MS. The reaction was quenched with water (100 mL) when it was complete. The aqueous solution was extracted with EtOAc (80 mL×3). The combined organic phase was washed with brine and concentrated to afford the crude product. The residue was purified by silica gel column (eluted with PE/EA=5:1 to 1:2) to afford compound 13 (4.8 g, 85.6% yield) as white oil. LC-MS: m/z 397 [M+1]+. 1H NMR (400 MHz, CDCl3): δ 8.00 (br. s, 1H), 7.70 (s, 1H), 7.65 (s, 1H), 7.34˜7.28 (m, 5H), 3.81 (s, 3H), 3.78˜3.72 (m, 2H), 3.41˜3.38 (m, 1H), 3.30˜3.24 (m, 2H), 3.14˜3.12 (m, 1H), 2.71˜2.67 (m, 1H), 2.58˜2.53 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09434733B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-0eb64468af20477ca88198566260bdf5 |
|---|
| Source note | uspto-grants-2016_09 |
|---|