反応 #4066913
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-e65a78bae07a476c844dc920e0e9e68a表示可能な構造データがありません
CCOC1(CC1)Br製品情報
1-bromo-1-ethoxycyclopropane (CAS 95631-62-2) 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 13380321
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
6 反応 · 6 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e65a78bae07a476c844dc920e0e9e68a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 1-benzyl-4-[N-methyl-N-(3-amino-2-pyridinyl)amino]piperidine (EXAMPLE 122, 825 mg), 1-bromo-1-ethoxycyclopropane (919 mg) and triethylamine (0.78 ml) in dry tetrahydrofuran (1.4 ml) under nitrogen is refluxed for 48 hrs, cooled to 20°-25°, diluted with methylene chloride (30 ml), washed with saline (10 ml), dried over sodium sulfate and concentrated under reduced pressure to give the crude product. The residue is chromatographed (silica gel, 70-230 mesh, 140 g; eluting with a gradient of methanol/methylene chloride (1/99-5/95)) to give the title compound, NMR (CDCl3) 7.80, 7.41, 7.25, 6.93, 5.62, 3.51, 3.48, 3.03, 2.87, 2.60, 1.98, 1.71, 1.64, 1.13 and 0.85δ. is refluxed for 48 hrs cooled to 20°-25° washed with saline (10 ml) dried over sodium sulfate concentrated under reduced pressure to give the crude product The residue is chromatographed (silica gel, 70-230 mesh, 140 g eluting with a gradient of methanol/methylene chloride (1/99-5/95))
ソース ID: ord-24bb735a9e6a41e986e4d7d6a9af0f11反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 1-benzyl-4-[N-methyl-N-(3-amino-2-pyridinyl)amino]piperidine (EXAMPLE 122, 825 mg), 1-bromo-1-ethoxycyclopropane (919 mg) and triethylamine (0.78 ml) in dry tetrahydrofuran (1.4 ml) under nitrogen is refluxed for 48 hrs, cooled to 20°-25°, diluted with methylene chloride (30 ml), washed with saline (10 ml), dried over sodium sulfate and concentrated under reduced pressure to give the crude product. The residue is chromatographed (silica gel, 70-230 mesh, 140 g; eluting with a gradient of methanol/methylene chloride (1/99-5/95)) to give the title compound, NMR (CDCl3) 7.80, 7.41, 7.25, 6.93, 5.62, 3.51, 3.48, 3.03, 2.87, 2.60, 1.98, 1.71, 1.64, 1.13 and 0.85δ. is refluxed for 48 hrs cooled to 20°-25° washed with saline (10 ml) dried over sodium sulfate concentrated under reduced pressure to give the crude product The residue is chromatographed (silica gel, 70-230 mesh, 140 g eluting with a gradient of methanol/methylene chloride (1/99-5/95))
ソース ID: ord-24bb735a9e6a41e986e4d7d6a9af0f11反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 1-benzyl-4-[N-methyl-N-(3-amino-2-pyridinyl)amino]piperidine (EXAMPLE 122, 825 mg), 1-bromo-1-ethoxycyclopropane (919 mg) and triethylamine (0.78 ml) in dry tetrahydrofuran (1.4 ml) under nitrogen is refluxed for 48 hrs, cooled to 20°-25°, diluted with methylene chloride (30 ml), washed with saline (10 ml), dried over sodium sulfate and concentrated under reduced pressure to give the crude product. The residue is chromatographed (silica gel, 70-230 mesh, 140 g; eluting with a gradient of methanol/methylene chloride (1/99-5/95)) to give the title compound, NMR (CDCl3) 7.80, 7.41, 7.25, 6.93, 5.62, 3.51, 3.48, 3.03, 2.87, 2.60, 1.98, 1.71, 1.64, 1.13 and 0.85δ. is refluxed for 48 hrs cooled to 20°-25° washed with saline (10 ml) dried over sodium sulfate concentrated under reduced pressure to give the crude product The residue is chromatographed (silica gel, 70-230 mesh, 140 g eluting with a gradient of methanol/methylene chloride (1/99-5/95))
ソース ID: ord-24bb735a9e6a41e986e4d7d6a9af0f11反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e65a78bae07a476c844dc920e0e9e68a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 1-benzyl-4-[N-methyl-N-(3-amino-2-pyridinyl)amino]piperidine (EXAMPLE 122, 825 mg), 1-bromo-1-ethoxycyclopropane (919 mg) and triethylamine (0.78 ml) in dry tetrahydrofuran (1.4 ml) under nitrogen is refluxed for 48 hrs, cooled to 20°-25°, diluted with methylene chloride (30 ml), washed with saline (10 ml), dried over sodium sulfate and concentrated under reduced pressure to give the crude product. The residue is chromatographed (silica gel, 70-230 mesh, 140 g; eluting with a gradient of methanol/methylene chloride (1/99-5/95)) to give the title compound, NMR (CDCl3) 7.80, 7.41, 7.25, 6.93, 5.62, 3.51, 3.48, 3.03, 2.87, 2.60, 1.98, 1.71, 1.64, 1.13 and 0.85δ. is refluxed for 48 hrs cooled to 20°-25° washed with saline (10 ml) dried over sodium sulfate concentrated under reduced pressure to give the crude product The residue is chromatographed (silica gel, 70-230 mesh, 140 g eluting with a gradient of methanol/methylene chloride (1/99-5/95))
ソース ID: ord-24bb735a9e6a41e986e4d7d6a9af0f11PubChem 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。
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