참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 1-Chloro-4-iodobenzene | HCID 12510 | — |
| 반응물 | Sodium Azide | HCID 33557 | — |
| 반응물 | L-Proline | HCID 145742 | — |
| 반응물 | 2-Ethynylthiophene | HCID 5246258 | — |
| 반응물 | Sodium Ascorbate | HCID 23667548 | — |
| 용매 | (Methanesulfinyl)methane--water (1/1) | HCID 23503278 | — |
| 생성물 | 1-(4-chloro-phenyl)-4-(thiophen-2-yl)-1H-1,2,3-triazole | HCID 86303656 | 5.5% |
반응 단계
A sealed tube was sequentially charged with 2-ethynylthiophene (250 mg, 2.31 mol), 1-chloro-4-iodobenzene (551 mg, 2.31 mmol, 1.0 eq.), L-proline (53 mg, 0.462 mmol, 0.2 eq.), Na2CO3 (50 mg, 0.462 mmol, 0.2 eq.), sodium ascorbate (91 mg, 0.462 mmol, 0.2 eq.), and 4 mL of DMSO:H2O (9:1). Then NaN3 (180 mg 2.77 mmol, 1.2 eq.) and CuSO4.5H2O (58 mg. 0.231 mmol, 0.1 eq.) were added, and the vessel was sealed. The suspension was stirred at 65° C. for 16 hours. The reaction mixture was then poured into ice-water and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over Na2SO4, and concentrated under vacuum. The crude product was then purified by silica column (100-200) using 15-20% ethyl acetate/hexanes to yield 1-(4-chloro-phenyl)-4-(thiophen-2-yl)-1H-1,2,3-triazole as a brown solid compound (34 mg, 0.13 mmol yield 5.5%). LC-MS [M+H] 261.8 (C12H8ClN3S+H, expected 262.01). The 1H-NMR spectra was in accordance with the chemical structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09402397B2 |
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| 출처 데이터셋 | uspto-grants-2016_08 |
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| ORD ID | ord-76a6409c3fb74f2d883e987204d32a0e |
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| 출처 메모 | uspto-grants-2016_08 |
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