HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009891Generated: October 30, 2026
Tris(hydroxymethyl)aminomethane → HCID 67304415, compound
https://huagongshe.com/reaction/1009891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 67303976 | HCID 67303976 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67304415 | HCID 67304415 | 35% |
Reaction Steps
To a chloroform solution (300 μL) of 1,1′-carbonyldiimidazole (7.30 mg, 0.045 mmol) were added a chloroform solution (150 μL) of (1S)-1-[5-[4-(2-aminoethyl)benzyl]-2-acetoxy-4-methylphenyl]-1,5-anhydro-2,3,4,6-tetra-O-acetyl-D-glucitol (18.4 mg, 0.030 mmol) and N-methyl morpholine (4.95 μL, 0.045 mmol), and the mixture was stirred for 30 minutes at room temperature. After that, to this reaction solution were added tris(hydroxymethyl)aminomethane (10.9 mg, 0.09 mmol) and N,N-dimethylformamide (150 μL), and this reaction mixture was stirred at 60° C. overnight. After the reaction mixture was cooled to room temperature, ethyl acetate was added thereto. And the mixture was washed with water, 1 M hydrochloric acid, and brine, and dried with anhydrous magnesium sulfate. The drying agent was filtered off, and the solvent was evaporated under reduced pressure. Thus obtained residue was purified with silica gel column chromatography (chloroform:methanol=95:5) to obtain the title compound (7.9 mg, 35%) as a colorless amorphous compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973012B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-56caeeacece84161920f8ee6859b240a |
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| Source note | uspto-grants-2011_07 |
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