HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972330Generated: November 1, 2026
Diisopropylethylamine → HCID 57872113, compound
https://huagongshe.com/reaction/1972330
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 | (2S,3S)-3-Amino-N-cyclopropyl-2-hydroxyhexanamide | HCID 16739337 | — |
| Reactant | HCID 69016469 | HCID 69016469 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57872113 | HCID 57872113 | 78.8% |
Reaction Steps
To a solution of (2S,4R)-1-(tert-butoxycarbonyl)-4-(7-methoxy-2-(1H-pyrazol-1-yl)quinolin-4-yloxy)pyrrolidine-2-carboxylic acid (5.0 g, 11.0 mmol) dissolved in a mixture of methylene chloride (135 mL) and N,N-dimethylformamide (45 mL) was added 2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU, (4.97 g, 42.6 mmol) and diisopropylethylamine (7.2 mL, 41.11 mmol), followed by the hydrochloride salt of (2S,3S)-3-amino-N-cyclopropyl-2-hydroxyhexanamide (2.45 g, 11.0 mmol). The reaction mixture was stirred at room temperature for 2 hours under nitrogen atmosphere. Completion of reaction was monitored by TLC. The reaction mixture was diluted with methylene chloride (200 mL) and washed with 10% hydrochloric acid (100 mL), followed by with 10% sodium bicarbonate solution (100 mL), water (100 mL) and brine (100 mL). The organic layer was dried over sodium sulfate, filtered, and the filtrate concentrated under reduced pressure to provide 5.4 g (67.6%) of (2S,4R)-tert-butyl 2-((2S,3S)-1-(cyclopropylamino)-2-hydroxy-1-oxohexan-3-ylcarbamoyl)-4-(7-methoxy-2-(1H-pyrazol-1-yl)quinolin-4-yloxy)pyrrolidine-1-carboxylate as an off-white solid (HPLC purity: 98.59% by area, HPLC retention time: 14.74 minutes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431733B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-022dac5166204a39bb9b44932b2d9d60 |
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| Source note | uspto-grants-2013_04 |
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