反応 #3877547
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f3626ec6050f4a15a01e658f55dcc44e表示可能な構造データがありません
CNC(=O)C1=C(C=CC(=C1)I)F製品情報
2-fluoro-5-iodo-N-methylbenzamide (CAS 866683-76-3) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 67047674
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
8 反応 · 8 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f3626ec6050f4a15a01e658f55dcc44e反応条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add bis(triphenylphosphine)palladium (II) dichloride (64 mg, 0.091 mmol), copper (I) iodide (35 mg, 0.19 mmol), and 3-ethynyl-5-methoxypyridine, (prepared as described in PREPARATION 10), (250 mg, 1.9 mmol) to a solution of 2-fluoro-5-iodo-N-methylbenzamide, (prepared as described in PREPARATION 39), (0.63 g, 2.3 mmol) in triethylamine (3.8 mL, 27.3 mmol) and heat at 60° C. for 16 h. Cool to room temperature and concentrate. Purify by silica gel chromatography, eluting with 100:0 to 10:90 dichloromethane:ethyl acetate, followed by a second silica gel chromatography eluting with 50:50 to 75:25 ethyl acetate:hexanes, to give the title compound as a white solid (390 mg, 73%). Cool to room temperature concentrate Purify by silica gel chromatography eluting with 100:0 to 10:90 dichloromethane eluting with 50:50 to 75:25 ethyl acetate
ソース ID: ord-3a7a95c0274745b6acf7bd43e1d02e2a反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add bis(triphenylphosphine)palladium (II) dichloride (45 mg, 0.06 mmol), copper (I) iodide (26 mg, 0.14 mmol), and 3-chloro-5-ethynylpyridine, (prepared as described in PREPARATION 27), (200 mg, 1.45 mmol) to a solution of 2-fluoro-5-iodo-N-methylbenzamide, (prepared as described in PREPARATION 39), (0.39 g, 1.39 mmol) in triethylamine (6 mL, 43 mmol) and heat at 70° C. After 10 min, add toluene (10 mL) to the solidified reaction mixture and heat at 70° C. for 1 h. Concentrate and purify using silica gel chromatography, eluting with 40:60 ethyl acetate:hexanes, to give the title compound as a white solid (300 mg, 72%). heat at 70° C. for 1 h Concentrate purify eluting with 40:60 ethyl acetate
ソース ID: ord-5cbc8d4ccddb4e09842d9b8af55b7fd8反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add bis(triphenylphosphine)palladium (II) dichloride (45 mg, 0.06 mmol), copper (I) iodide (26 mg, 0.14 mmol), and 3-chloro-5-ethynylpyridine, (prepared as described in PREPARATION 27), (200 mg, 1.45 mmol) to a solution of 2-fluoro-5-iodo-N-methylbenzamide, (prepared as described in PREPARATION 39), (0.39 g, 1.39 mmol) in triethylamine (6 mL, 43 mmol) and heat at 70° C. After 10 min, add toluene (10 mL) to the solidified reaction mixture and heat at 70° C. for 1 h. Concentrate and purify using silica gel chromatography, eluting with 40:60 ethyl acetate:hexanes, to give the title compound as a white solid (300 mg, 72%). heat at 70° C. for 1 h Concentrate purify eluting with 40:60 ethyl acetate
ソース ID: ord-5cbc8d4ccddb4e09842d9b8af55b7fd8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add methylamine hydrochloride (0.57 g, 8.4 mmol) and triethylamine (2.17 mL, 15.5 mmol) to a solution of 2-fluoro-5-iodobenzoyl chloride (2.0 g, 7.0 mmol) in dichloromethane (100 mL) at 0° C. Warm to room temperature and stir 20 h. Concentrate and purify by silica gel chromatography, eluting with a gradient of 75:25 to 60:40 hexanes:ethyl acetate, to give the title compound as a white solid (1.7 g, 87%). Concentrate purify by silica gel chromatography eluting with a gradient of 75:25 to 60:40 hexanes
ソース ID: ord-8e951beab54c4d9cb3135a70879e971c反応条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add bis(triphenylphosphine)palladium (II) dichloride (64 mg, 0.091 mmol), copper (I) iodide (35 mg, 0.19 mmol), and 3-ethynyl-5-methoxypyridine, (prepared as described in PREPARATION 10), (250 mg, 1.9 mmol) to a solution of 2-fluoro-5-iodo-N-methylbenzamide, (prepared as described in PREPARATION 39), (0.63 g, 2.3 mmol) in triethylamine (3.8 mL, 27.3 mmol) and heat at 60° C. for 16 h. Cool to room temperature and concentrate. Purify by silica gel chromatography, eluting with 100:0 to 10:90 dichloromethane:ethyl acetate, followed by a second silica gel chromatography eluting with 50:50 to 75:25 ethyl acetate:hexanes, to give the title compound as a white solid (390 mg, 73%). Cool to room temperature concentrate Purify by silica gel chromatography eluting with 100:0 to 10:90 dichloromethane eluting with 50:50 to 75:25 ethyl acetate
ソース ID: ord-3a7a95c0274745b6acf7bd43e1d02e2a反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add bis(triphenylphosphine)palladium (II) dichloride (45 mg, 0.06 mmol), copper (I) iodide (26 mg, 0.14 mmol), and 3-chloro-5-ethynylpyridine, (prepared as described in PREPARATION 27), (200 mg, 1.45 mmol) to a solution of 2-fluoro-5-iodo-N-methylbenzamide, (prepared as described in PREPARATION 39), (0.39 g, 1.39 mmol) in triethylamine (6 mL, 43 mmol) and heat at 70° C. After 10 min, add toluene (10 mL) to the solidified reaction mixture and heat at 70° C. for 1 h. Concentrate and purify using silica gel chromatography, eluting with 40:60 ethyl acetate:hexanes, to give the title compound as a white solid (300 mg, 72%). heat at 70° C. for 1 h Concentrate purify eluting with 40:60 ethyl acetate
ソース ID: ord-5cbc8d4ccddb4e09842d9b8af55b7fd8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Add methylamine hydrochloride (0.57 g, 8.4 mmol) and triethylamine (2.17 mL, 15.5 mmol) to a solution of 2-fluoro-5-iodobenzoyl chloride (2.0 g, 7.0 mmol) in dichloromethane (100 mL) at 0° C. Warm to room temperature and stir 20 h. Concentrate and purify by silica gel chromatography, eluting with a gradient of 75:25 to 60:40 hexanes:ethyl acetate, to give the title compound as a white solid (1.7 g, 87%). Concentrate purify by silica gel chromatography eluting with a gradient of 75:25 to 60:40 hexanes
ソース ID: ord-8e951beab54c4d9cb3135a70879e971cPubChem References
化合物の公開データベース記録に掲載された情報源です。
関連製品
12 related records
CAS 331434-64-1
CAS 1261827-65-9
CAS 1315689-04-3
CAS 724-37-8
CAS 712301-16-1
CAS 2586-34-7
CAS 948717-18-8
CAS 613678-12-9
CAS 710318-32-4
CAS 1872794-09-6
CAS 1369790-97-5
CAS 349129-43-7
見積依頼
仕様、数量、納入先、用途をご連絡ください。供給可否を確認します。
