HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240862Generated: October 30, 2026
Diisopropylethylamine → HCID 50991923, compound
https://huagongshe.com/reaction/240862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 50991845 | HCID 50991845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 50991923 | HCID 50991923 | 24% |
Reaction Steps
O-(7-Azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (HATU; 63 mg, 0.167 mmol) was added to a mixture solution of 4-(6-(4-methoxyphenyl)-1-(6-(methylamino)pyrimidin-4-yl)-1H-indol-3-yl)benzoate (50 mg, 0.111 mmol), 2-morpholinoethanamine (14.6 μL, 0.111 mmol) and diisopropylethylamine (DIPEA; 29 μL, 0.167 mmol) in THF (2 mL) at room temperature. 2 hours later, the mixture was added to saturated sodium bicarbonate aqueous solution and then extracted with methylene chloride. The collected organic layer was washed with brine and concentrated under reduced pressure by drying with anhydrous magnesium sulfate. The residue was purified by chromatography (preparative HPLC). The target compound (15 mg) was obtained as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-5228dfb5991b41c1a4c21746b2862ba4 |
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| Source note | uspto-grants-2014_02 |
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