HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173758Generated: October 30, 2026
Acetic Acid → Methyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate
https://huagongshe.com/reaction/2173758
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | Tert-butyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate | HCID 66716290 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate | HCID 66714165 | 26.6% |
Reaction Steps
To a solution of 670 mg of tert-butyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate in 20 ml of DCM was added 2 ml of TFA. The mixture was stirred for 6 hours at room temperature and then concentrated under reduced pressure, taken up in DCM and concentrated again under reduced pressure. To the residue obtained, dissolved in 10 ml of MeOH, was added, at 5° C., 7 ml of a 2M solution of (trimethylsilyl)diazomethane in hexane. The mixture was stirred for 1 hour 30 minutes at 5° C. and then 200 μl of acetic acid were added. The mixture was taken up in 30 ml of water and 30 ml of EtOAc. The aqueous phase was extracted 2× with 30 ml of EtOAc. The organic phases were combined, washed with saturated NaCl solution, concentrated under reduced pressure and purified by flash chromatography on silica (Analogix Super Flash SiO2 SF15-24g), using a gradient of 0 to 10% MeOH in DCM. The fractions containing the desired product were combined and concentrated under reduced pressure. 155 mg of methyl 3-[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethylamino]-propanoate were obtained. LC/MS (C): tr=2.56 min; [M+H]+: m/z 470.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056914B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-840cb5b71dc34c368aa3a1024273d0b0 |
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| Source note | uspto-grants-2015_06 |
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