Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Reactant | sodium L-ascorbic acid | HCID 66586226 | — |
| Reactant | tert-butyl N-but-3-ynyl-N-[2-[2-(indan-2-ylamino)-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl]-2-oxo-ethyl]carbamate | HCID 86726552 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178453339 | HCID 178453339 | 63.3% |
Reaction Steps
Add copper(II)sulfate pentahydrate (0.026 g; 0.2 equiv; 0.106 mmoles) and L-ascorbic acid sodium salt (0.21 g; 2.0 equiv; 1.06 mmoles) to a deoxygenated solution of tert-butyl N-but-3-ynyl-N-[2-[2-(indan-2-ylamino)-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl]-2-oxo-ethyl]carbamate (0.252 g; 1.0 equiv; 0.53 mmoles) in dimethylformamide (6 mL) and water (3 mL) (including toluene (0.05 mL) as an internal standard). Heat the reaction vessel to 90° C. and then add azidotrimethylsilane (0.565 mL; 8 equiv; 4.24 mmoles) slowly. Stir at 90° C. for 4 hours, then dilute the reaction mixture with water (100 mL) and ethyl acetate (50 mL), and extract 3×50 mL ethyl acetate. Wash the combined organic extracts with brine, dry over magnesium sulfate, filter, and concentrate. Purify the crude product by column chromatography (0 to 10% methanol in ethyl acetate) to give tert-butyl {2-[2-(2,3-dihydro-1H-inden-2-ylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl]-2-oxoethyl}[2-(1H-1,2,3-triazol-4-yl)-ethyl]carbamate (0.174 g; 63%) as a colorless foam: MS (m/z): 519 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08969555B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-807e6e7eb6c84947bd27e8c3e1ad1da6 |
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| Source note | uspto-grants-2015_03 |
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