HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952867Generated: November 1, 2026
Tris(hydroxymethyl)aminomethane → HCID 11428128, compound
https://huagongshe.com/reaction/1952867
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | HCID 11323531 | HCID 11323531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | N-Cyclohexylcarbodiimide | HCID 12048208 | — |
| Solvent | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Product | HCID 11428128 | HCID 11428128 | — |
Reaction Steps
To a solution of isobutyrric acid (49 μl, 0.53 mmol) in CH2Cl2 (1.5 ml), N-cyclohexylcarbodiimide, N'-methyl polystyrene (0.4 g, loading 2 mmol/g, 0.798 mmol), Nhydroxybenzotriazole (0.072 g, 0.53 mmol) and a solution of 2-(2-amino-1,3-thiazol-4-yl)-N-(5-isopropyl-1,3-thiazol-2-yl)acetamide (0.075 g, 0.266 mmol) in CH2Cl2 /DMF (0.4 ml/0.6 ml) were added. The reaction mixture was maintained under stirring at room temperature for about 8 days. After this time, PS-Trisamine (0.44 g, loading 3.62 mmol/g, 1.596 mmol) was added, stirring was continued for about 6 hours and then the mixture was filtered. The resin was washed with CH2Cl2 (1 ml×5), the organic layers were combined and evaporated to dryness to give, after trituration with diisopropyl ether the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06114365 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-9b7131b03ab04a2f9535772303f209a6 |
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| Source note | uspto-grants-2000_09 |
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