HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206380Generated: October 31, 2026
2-Dimethylaminopyridine → HCID 86704072, compound
https://huagongshe.com/reaction/2206380
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-N-Boc-aminopropionic acid | HCID 268471 | — |
| 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 72550676 | HCID 72550676 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86704072 | HCID 86704072 | 73% |
Reaction Steps
A mixture of (S)-L-(2-(tert-butoxycarbonylamino)propanoic acid (Chem-Impex, 13.6 mg, 0.072 mmol), HATU (Bachem, 27.3 mg, 0.072 mmol), N,N-diisopropylethylamine (18.6 mg, 0.025 mL, 0.144 mmol) and dimethylaminopyridine (Aldrich, 2.2 mg, 0.018 mmol) in dimethyl formamide (8 mL) was stirred for 10 min before 2-hydroxyethyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-3-methoxybenzoate (Example 1, 19 mg, 0.028 mmol) in dimethyl formamide (1 mL) was added. The reaction mixture was stirred overnight and then diluted with ethyl acetate, washed successively with aqueous sodium bicarbonate solution, water (3×15 mL) and brine (15 mL), dried over anhydrous sodium sulfate and concentrated. The crude material was purified by flash chromatography (hexane/ethyl acetate, 95/5 to 65/35) to give chiral 4-{[(2R,3S,4R,5S)-3-(3-chloro-2-fluoro-phenyl)-4-(4-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-3-methoxy-benzoic acid 2-((S)-2-tert-butoxycarbonylamino-propionyloxy)-ethyl ester as a white solid (17 mg, 71% yield). MS (ES+) m/z calcd. for C41H47Cl2F2N4O8 [(M+H)+]: 831. found: 831.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371280B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-52a7c57bd019420599ea26c1c40c3fd1 |
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| Source note | uspto-grants-2016_06 |
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