反应 #4043057
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-80bb4d33469a444aa2c0b183f9d56760暂无可渲染的结构数据
C1COC(=N1)N产品信息
4,5-二氢-1,3-恶唑-2-胺(CAS 24665-93-8)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-80bb4d33469a444aa2c0b183f9d56760反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to 2-amino-4,5-dihydrooxazole via Procedure G. The product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(4,5-dihydrooxazol-2-yl)terephthalamide. MS (Q1) 456 (M)+. The product was purified on reverse phase HPLC
来源 ID: ord-122c6799dbdb4cee965e995cdafe6626反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to 2-amino-4,5-dihydrooxazole via Procedure G. The product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(4,5-dihydrooxazol-2-yl)terephthalamide. The product was purified on reverse phase HPLC
来源 ID: ord-9264907009dc40caa43474a39948d9b9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to 2-amino-4,5-dihydrooxazole via Procedure G. The product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(4,5-dihydrooxazol-2-yl)terephthalamide. The product was purified on reverse phase HPLC
来源 ID: ord-9264907009dc40caa43474a39948d9b9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-80bb4d33469a444aa2c0b183f9d56760反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to 2-amino-4,5-dihydrooxazole via Procedure G. The product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(4,5-dihydrooxazol-2-yl)terephthalamide. MS (Q1) 456 (M)+. The product was purified on reverse phase HPLC
来源 ID: ord-1d2fad47b80c4915bc7f5ead36a6a6b0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to 2-amino-4,5-dihydrooxazole via Procedure G. The product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(4,5-dihydrooxazol-2-yl)terephthalamide. MS (Q1) 456 (M)+. The product was purified on reverse phase HPLC
来源 ID: ord-122c6799dbdb4cee965e995cdafe6626反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to 2-amino-4,5-dihydrooxazole via Procedure G. The product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(4,5-dihydrooxazol-2-yl)terephthalamide. The product was purified on reverse phase HPLC
来源 ID: ord-9264907009dc40caa43474a39948d9b9PubChem References
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