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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695202Generated: October 30, 2026

Tris(hydroxymethyl)aminomethane → HCID 67188392, compound

https://huagongshe.com/reaction/1695202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromovaleryl chlorideHCID 521173—
ReactantN-AcetylhomopiperazineHCID 4186202—
ReactantHCID 178507300HCID 178507300—
SolventDimethylacetamideHCID 31374—
ProductHCID 67188392HCID 6718839217%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163729B2
Source datasetuspto-grants-2012_04
ORD IDord-6cc6c255c98d4790a678596ad6f4ac53
Source noteuspto-grants-2012_04