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Triethylamine → N-({6-[(2-Fluoroethyl)amino]-4-(methylthio)pyridin-2-yl}carbamoyl)-5-(2-methoxyethyl)-4-methylthiophene-2-sulfonamide

HRID 1696746
ノート
印刷プレビュー

反応式

HRID 1696746 の反応式
[CH3:1][O:2][CH2:3][CH2:4][C:5]1[S:9][C:8]([S:10]([NH2:13])(=[O:12])=[O:11])=[CH:7][C:6]=1[CH3:14].Cl[C:16](OC1C=CC=CC=1)=[O:17].C(N(CC)CC)C.[F:32][CH2:33][CH2:34][NH:35][C:36]1[CH:41]=[C:40]([S:42][CH3:43])[CH:39]=[C:38]([NH2:44])[N:37]=1>C(#N)C>[F:32][CH2:33][CH2:34][NH:35][C:36]1[N:37]=[C:38]([NH:44][C:16]([NH:13][S:10]([C:8]2[S:9][C:5]([CH2:4][CH2:3][O:2][CH3:1])=[C:6]([CH3:14])[CH:7]=2)(=[O:12])=[O:11])=[O:17])[CH:39]=[C:40]([S:42][CH3:43])[CH:41]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 15891Phenyl chloroformateHCID 67274431HCID 67274431、化合物HCID 86630931HCID 86630931、化合物

生成物 1

HCID 42629873N-({6-[(2-Fluoroethyl)amino]-4-(methylthio)pyridin-2-yl}carbamoyl)-5-(2-methoxyethyl)-4-methylthiophene-2-sulfonamide収率 23.9%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒
2 回

反応条件

温度
60 °C

実験手順

5-(2-Methoxy-ethyl)-4-methyl-thiophene-2-sulfonic acid amide (0.063 g, 0.373 mmol) was dissolved in 2.2 mL of abs. acetonitrile and treated successively with phenyl chloroformate (0.058 g, 1.0 eq.) and triethylamine (0.129 mL, 2.5 eq.), and the mixture kept at ambient temperature for 1 h. The below prepared N-(2-fluoro-ethyl)-4-methylsulfanyl-pyridine-2,6-diamine (0.094 g, 1.0 eq.), dissolved in a tiny amount of acetonitrile, was then added, and the mixture heated to 60° C. for 18 h. Cooling, pouring onto crashed ice, twofold extraction with AcOEt, washing with water and brine, drying over sodium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, hexane/AcOEt=4/6) and crystallization from AcOEt, yielded eventually 0.041 g of the title compound as off-white crystals.

後処理

  1. additionwas then added
  2. temperatureCooling
  3. additionpouring
  4. extractionice, twofold extraction with AcOEt
  5. washwashing with water and brine
  6. dry with materialdrying over sodium sulfate, and evaporation of the solvents
  7. customfollowed by flash chromatography (SiO2, hexane/AcOEt=4/6) and crystallization from AcOEt

出典と根拠

ORDレコード
ord-0d1e6cb8e1dc46ea8aeb836f3cd6a1d8
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163778B2

反応ノート

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