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Ethanolamine → HCID 59406275、化合物

HRID 58055
ノート
印刷プレビュー

反応式

HRID 58055 の反応式
Cl.[Br:2][C:3]1[CH:4]=[CH:5][C:6]([S:9](Cl)(=[O:11])=[O:10])=[N:7][CH:8]=1.[NH2:13][CH2:14][CH2:15][OH:16].CCN(CC)CC>C(#N)C>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([S:9]([NH:13][CH2:14][CH2:15][OH:16])(=[O:11])=[O:10])=[N:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 700EthanolamineHCID 8471TriethylamineHCID 467388875-Bromopyridine-2-sulfonyl chloride, HCl

生成物 1

HCID 59406275HCID 59406275、化合物

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

In a 4 mL vial equipped with a magnetic stir bar were combined 5-bromopyridine-2-sulfonyl chloride hydrochloride (50 mg, 0.171 mmol), 2-aminoethanol (0.015 mL, 0.256 mmol), Et3N (0.071 mL, 0.512 mmol), and acetonitrile (1 mL). The resulting yellow solution stirred at room temperature overnight. The reaction mixture was subsequently partitioned between water (10 mL) and ethyl acetate (15 mL). The layers were separated and the aqueous layer was back-extracted with ethyl acetate (15 mL). The combined organic layers were concentrated to give the title compound as a clear liquid, which was used without further purification (55 mg).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customIn a 4 mL vial equipped with a magnetic stir bar
  2. customThe reaction mixture was subsequently partitioned between water (10 mL) and ethyl acetate (15 mL)
  3. customThe layers were separated
  4. extractionthe aqueous layer was back-extracted with ethyl acetate (15 mL)
  5. concentrationThe combined organic layers were concentrated

出典と根拠

ORDレコード
ord-cf474c12ee78446ea5f7e28f2d3e3706
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434743B2

反応ノート

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