反应 #4016380
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-9e41034fbd724c5db777084ec36d6936暂无可渲染的结构数据
CCOC(=O)CCCN=C=O产品信息
4-异氰酸基丁酸乙酯(CAS 106508-62-7)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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合成路线数据
9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e41034fbd724c5db777084ec36d6936反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-ylamine (Example 72), (0.1 g, 0.31 mmol) DIPEA (0.039 ml, 0.34 mmol), ethyl-4-isocyanatobutyrate (0.046 ml, 0.31 mmol) in DCM (2 ml) are heated together at reflux overnight. The reaction mixture is diluted with DCM (20 ml) and washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml), dried over MgSO4, filtered and concentrated in vacuo to yield the titled compound as an off white solid. at reflux overnight washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml) dried over MgSO4 filtered concentrated in vacuo
来源 ID: ord-87c2adc378b748ea86a9ec2a8f884ed2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-ylamine (Example 72), (0.1 g, 0.31 mmol) DIPEA (0.039 ml, 0.34 mmol), ethyl-4-isocyanatobutyrate (0.046 ml, 0.31 mmol) in DCM (2 ml) are heated together at reflux overnight. The reaction mixture is diluted with DCM (20 ml) and washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml), dried over MgSO4, filtered and concentrated in vacuo to yield the titled compound as an off white solid. at reflux overnight washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml) dried over MgSO4 filtered concentrated in vacuo
来源 ID: ord-87c2adc378b748ea86a9ec2a8f884ed2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e41034fbd724c5db777084ec36d6936反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-ylamine (Example 72), (0.1 g, 0.31 mmol) DIPEA (0.039 ml, 0.34 mmol), ethyl-4-isocyanatobutyrate (0.046 ml, 0.31 mmol) in DCM (2 ml) are heated together at reflux overnight. The reaction mixture is diluted with DCM (20 ml) and washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml), dried over MgSO4, filtered and concentrated in vacuo to yield the titled compound as an off white solid. at reflux overnight washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml) dried over MgSO4 filtered concentrated in vacuo
来源 ID: ord-704a95a01a334b7eb2d6fbfa17200dbb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The titled compound is prepared by an analogous procedure to 3-{3-[4-Methyl-5-(2-morpholin-4-yl-pyridin-4-yl)-thiazol-2-yl]-ureido}-propionic acid ethyl ester (Example 14) by replacing ethyl 3-isocyanatopropionate with 4-isocyanato-butyric acid ethyl ester.
来源 ID: ord-278ad8c893564d7a9cfc4d5625cfb9c5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-(4-Nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester (25 mg, 0.087 mmol, 1 molequivalent), prepared as described hereinabove (see, preparation of Compound 1), ethyl 4-isocyanatobutyrate (135 mg, 0.87 mmol) and triethylamine (214 μl, 1.74 mmol) were stirred overnight at room temperature. Additional 4-isocyanatobutyrate (130 μl) was added and the mixture was heated to 50° C. and was stirred at this temperature overnight. Once TLC analysis, using a 2:1 hexane:ethyl acetate mixture as eluent, indicated a complete conversion, the crude mixture was purified by column chromatography using a gradient of hexane to hexane:ethyl acetate (9:1) as eluent to give pure Compound 30 (26 mg, 74% yield). the mixture was heated to 50° C. was stirred at this temperature overnight the crude mixture was purified by column chromatography
来源 ID: ord-e4a13dcc3813461088139e50413ed0c5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-ylamine (Example 72), (0.1 g, 0.31 mmol) DIPEA (0.039 ml, 0.34 mmol), ethyl-4-isocyanatobutyrate (0.046 ml, 0.31 mmol) in DCM (2 ml) are heated together at reflux overnight. The reaction mixture is diluted with DCM (20 ml) and washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml), dried over MgSO4, filtered and concentrated in vacuo to yield the titled compound as an off white solid. at reflux overnight washed with 1M hydrochloric acid (15 ml), water (2×15 ml), brine (15 ml) dried over MgSO4 filtered concentrated in vacuo
来源 ID: ord-87c2adc378b748ea86a9ec2a8f884ed2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e41034fbd724c5db777084ec36d6936PubChem 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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