反应 #4151646
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-f26fb7042f1547e3b3077d965776a816暂无可渲染的结构数据
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f26fb7042f1547e3b3077d965776a816反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7946979a49b245c6a28f37d503e66ece反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-01123dbb1eea4f0ca582cd558fc37de7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1a7e42075b464959b9780a6f2887c63d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f26fb7042f1547e3b3077d965776a816反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7946979a49b245c6a28f37d503e66ece反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-01123dbb1eea4f0ca582cd558fc37de7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1a7e42075b464959b9780a6f2887c63d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-{5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-3-methyl-1H-indazol-5-ylmethylene]-4-oxo-4,5-dihydro-thiazol-2-yl}-2-hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester was prepared from 5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-3-methyl-1H-indazol-5-ylmethylene]-2-ethylsulfanyl-thiazol-4-one and 2-Hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester following General Procedure C.
来源 ID: ord-6e59a96f47cf45a586660d16bba360cd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-{5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-4-oxo-4,5-dihydro-thiazol-2-yl}-2-(R)-hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester was prepared from 5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-2-ethylsulfanyl-thiazol-4-one and 2-Hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester following General Procedure B.
来源 ID: ord-5e1f5fc608df456084d724ee9e8011d4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-{5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-3-methyl-1H-indazol-5-ylmethylene]-4-oxo-4,5-dihydro-thiazol-2-yl}-2-hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester was prepared from 5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-3-methyl-1H-indazol-5-ylmethylene]-2-ethylsulfanyl-thiazol-4-one and 2-Hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester following General Procedure C.
来源 ID: ord-0104ce35a1ca4728b60d5e48b33bb77c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-{5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-4-oxo-4,5-dihydro-thiazol-2-yl}-2-(R)-hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester was prepared from 5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-2-ethylsulfanyl-thiazol-4-one and 2-Hydroxymethyl-piperazine-1-carboxylic acid tert-butyl ester following General Procedure B.
来源 ID: ord-e4a6094c95bc46609b0b75e18e0bbf9cPubChem References
以下资料来自该化合物的公开数据库参考记录。
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