HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881701Generated: November 1, 2026
Diisopropylethylamine → HCID 44464593, compound
https://huagongshe.com/reaction/1881701
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 57916232 | HCID 57916232 | — |
| Reactant | HCID 57916235 | HCID 57916235 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44464593 | HCID 44464593 | 60% |
Reaction Steps
DIPEA (2 eq.) and HATU (1.2 eq.) were added to a solution of tetrahydrofuran and 2-(2-(2-chloro-N-cyclopropyl-6-methylphenylsulfonamido)ethoxy)acetic acid [acid K] (1 eq.) at 0° C. 4-(3-Fluorophenyl)-4-(2-(pyrrolidin-1-yl)ethoxy)piperidine [amine C] (1.2 eq.) was taken up in tetrahydrofuran (2 ml/mmol) and the solution was rendered basic with DIPEA (2 eq.) and added to the reaction mixture at 0° C. The reaction mixture was stirred at 25° C. for 16 h. The mixture was concentrated to dryness on a rotary evaporator, the residue was taken up in methylene chloride and the mixture was washed with water and sat. sodium chloride solution and dried over sodium sulfate. The organic phase was concentrated and the crude product was purified by means of column chromatography (5% methanol in methylene chloride). Yield: 60%. MS, Rt=3.6 min, m/z=622.4 [MH]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318769B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-1ec14f126924450088744dc979215677 |
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| Source note | uspto-grants-2012_11 |
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