HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962860Generated: October 25, 2026
Ammonium Chloride → 2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamide
https://huagongshe.com/reaction/1962860
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 2-Amino-3-methoxy-2-methylpropan-1-ol | HCID 13375415 | — |
| Reactant | (3-Ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acid | HCID 59565474 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamide | HCID 59565371 | 35.4% |
Reaction Steps
(3-Ethynyl-quinolin-6-yloxy)-methylsulfanyl-acetic acid (413 mg), 1-hydroxy-7-azabenzotriazole (HOAT) (267 mg), O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU) (630 mg), 2-amino-3-methoxy-2-methyl-propan-1-ol (180 mg) and triethylamine (0.75 ml) in dry CH3CN (20 ml) were stirred at ambient temperature overnight. The reaction mixture was diluted with ethyl acetate and poured on sat. aq. NH4Cl. The water phase was extracted 3 times with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and evaporated. The residue was purified by column chromatography (cyclohexane/ethyl acetate 1:1) to give as a yellowish oil 2-(3-Ethynyl-quinolin-6-yloxy)-N-(2-hydroxy-1-methoxymethyl-1-methyl-ethyl)-2-methylsulfanyl-acetamide (200 mg) as a mixture of diastereoisomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415272B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-ac84d842a74f41018a2c4cb78c4fc1ed |
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| Source note | uspto-grants-2013_04 |
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