HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853653Generated: October 30, 2026
Diisopropylethylamine → HCID 68929461, compound
https://huagongshe.com/reaction/853653
Participants
| Role | Name | HCID | Charge |
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| 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 58928692 | HCID 58928692 | — |
| Reactant | HCID 86593996 | HCID 86593996 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68929461 | HCID 68929461 | 45.6% |
Reaction Steps
A solution of 13.5 mg of 213 in 0.13 mL of DMF was stirred with HATU (20 mg, 0.052 mmol) at room temperature for 10 minutes. To this solution was added a premixed solution of 219 (28 mg, 0.078 mmol) of approximately 50% purity in 0.130 mL of DMF and DIEA (13.4 mg, 0.104 mmol). The reaction mixture was gently heated with a heat gun for 30 seconds and then the reaction was allowed to proceed at room temperature for 2 hours when LCMS demonstrated complete consumption of the carboxylic acid. The reaction mixture was loaded onto a silica gel column and purified with EtOAc-10% MeOH to provide 9.5 mg of 3-[(2-{[9-Benzhydryloxy-7-(4-fluoro-benzyl)-8-oxo-7,8-dihydro-6H-pyrrolo[3,4-g]quinoline-5-carbonyl]-amino}-ethyl)-phenoxy-phosphinoyl]-2-methyl-propionic acid ethyl ester 220 which was carried on to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253180B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-851e88a4686b4dce9f8559e156826c56 |
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| Source note | uspto-grants-2007_08 |
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