ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Sodium Azide → 5-(4-Chlorophenyl)-4-(3,3,3-trifluoro-2-hydroxypropyl)-2-({1-[3-(trifluoromethyl)benzyl]-1H-1,2,3-triazol-4-yl}methyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

HRID 714709
ノート
印刷プレビュー

反応式

HRID 714709 の反応式
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH2:6]Br.[N-:13]=[N+:14]=[N-:15].[Na+].[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([C:24]2[N:25]([CH2:33][CH:34]([OH:39])[C:35]([F:38])([F:37])[F:36])[C:26](=[O:32])[N:27]([CH2:29][C:30]#[CH:31])[N:28]=2)=[CH:20][CH:19]=1>C(#N)C.O.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([C:24]2[N:25]([CH2:33][CH:34]([OH:39])[C:35]([F:37])([F:38])[F:36])[C:26](=[O:32])[N:27]([CH2:29][C:30]3[N:13]=[N:14][N:15]([CH2:6][C:5]4[CH:8]=[CH:9][CH:10]=[C:3]([C:2]([F:12])([F:11])[F:1])[CH:4]=4)[CH:31]=3)[N:28]=2)=[CH:20][CH:19]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 33557Sodium AzideHCID 1230611-(Bromomethyl)-3-(trifluoromethyl)benzeneHCID 866909095-(4-Chlorophenyl)-2-(prop-2-yn-1-yl)-4-(3,3,3-trifluoro-2-hydroxypropyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

生成物 1

HCID 866909325-(4-Chlorophenyl)-4-(3,3,3-trifluoro-2-hydroxypropyl)-2-({1-[3-(trifluoromethyl)benzyl]-1H-1,2,3-triazol-4-yl}methyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

試薬・触媒・溶媒 2

HCID 165397
Cupric acetate monohydrate
触媒
HCID 6342Acetonitrile溶媒

実験手順

29 mg (0.12 mmol) of 3-(trifluoromethyl)benzyl bromide were initially charged in 1 ml of acetonitrile, and 8 mg (0.12 mmol) of sodium azide were added. The mixture was stirred at RT for 1 h. 0.24 mg (0.012 mmol) of copper(II) acetate monohydrate and 50 mg (0.14 mmol) of the compound from Example 13A were then added. The resulting mixture was stirred at room temperature for 11 days. The reaction mixture was then filtered through a little silica gel, the product being eluted with about 10 ml of ethyl acetate, and the filtrate was concentrated under reduced pressure. The crude product was purified chromatographically [Method 19]. This gave 52 mg (65% of theory) of the target compound.

後処理

  1. stirringThe resulting mixture was stirred at room temperature for 11 days
  2. filtrationThe reaction mixture was then filtered through a little silica gel
  3. washthe product being eluted with about 10 ml of ethyl acetate
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customThe crude product was purified chromatographically [Method 19]

出典と根拠

ORDレコード
ord-b402b7c0f8ec44798cb93f67b9a84440
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187466B2

反応ノート

読み込み中…

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