HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695202Generated: October 30, 2026
Tris(hydroxymethyl)aminomethane → HCID 67188392, compound
https://huagongshe.com/reaction/1695202
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromovaleryl chloride | HCID 521173 | — |
| Reactant | N-Acetylhomopiperazine | HCID 4186202 | — |
| Reactant | HCID 178507300 | HCID 178507300 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 67188392 | HCID 67188392 | 17% |
Reaction Steps
Bromovaleryl chloride (1.62 mL, 12.12 mmol) was dissolved in DMA (50 mL). To this, a solution of 5-thiophen-2-yl-2H-pyrazol-3-ylamine (2 g, 12.12 mmol) and DIEA (2.1 mL, 12.12 mmol) was added portionwise at 0° C. The reaction mixture was left stirring 1 hour at 0° C. and then for 2 hours at room temperature. After a total of 3 hours, PS-Trisamine (1 g, ˜4 mmol/g) was added to the mixture and left stirring for 2 hours. Then, N-acetylhomopiperazine (4.3 g, 30.3 mmol) was added and the mixture was left stirring at room temperature for a further 60 hours. After DMA evaporation under reduced pressure, water was added (50 mL) and this was extracted with ethyl acetate (3×30 mL). The aqueous layer was basified with solid NaOH and extracted with ethyl acetate at pH=10 and then again at pH=11. All the organic phases were reunited, dried and evaporated. The residue was purified by silica chromatography eluting with a gradient of ethyl acetate/methanol 9:1 up to ethyl acetate/methanol 8:2, to give the title compound as yellowish oil (800 mg, 17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163729B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-6cc6c255c98d4790a678596ad6f4ac53 |
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| Source note | uspto-grants-2012_04 |
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