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Acetic Anhydride → 4-[1-[1-[Bis(4-fluorophenyl)methyl]piperazin-4-yl]-2-acetoxy-3-propanylthio]pyridine

HRID 1586700
ノート
印刷プレビュー

反応式

HRID 1586700 の反応式
[SH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[CH2:16][CH:17]([OH:40])[CH2:18][N:19]1[CH2:24][CH2:23][N:22]([CH:25]([C:33]2[CH:38]=[CH:37][C:36]([F:39])=[CH:35][CH:34]=2)[C:26]2[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=2)[CH2:21][CH2:20]1.[C:41](OC(=O)C)(=[O:43])[CH3:42]>CN(C=O)C.C(Cl)Cl.CO>[F:32][C:29]1[CH:30]=[CH:31][C:26]([CH:25]([C:33]2[CH:38]=[CH:37][C:36]([F:39])=[CH:35][CH:34]=2)[N:22]2[CH2:23][CH2:24][N:19]([CH2:18][CH:17]([O:40][C:41](=[O:43])[CH3:42])[CH2:16][S:1][C:2]3[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=3)[CH2:20][CH2:21]2)=[CH:27][CH:28]=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

8

反応物 4

HCID 7918Acetic AnhydrideHCID 8471Triethylamine2 回HCID 103851541-(1-Chloro-2-hydroxy-3-propanyl)-4-(4,4'-difluorobenzhydryl)piperazineHCID 178418431pyridine-4-thiol

生成物 1

HCID 541635124-[1-[1-[Bis(4-fluorophenyl)methyl]piperazin-4-yl]-2-acetoxy-3-propanylthio]pyridine収率 15.3%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒
HCID 6228Dimethylformamide溶媒2 回
HCID 6344Dichloromethane溶媒3 回

反応条件

温度
60 °C

実験手順

To 4-mercaptopyridine (0.555 g, 5 mmol) in DMF (5 mL) with triethylamine (0.7 mL, 5 mmol) was added 1-(1-chloro-2-hydroxy-3-propanyl)-4-(4, 4'-difluorobenzhydryl) piperazine (1.91 g, 5 mmol) in DMF (15 mL) dropwise over 15 minutes under nitrogen. After 8 days, the reaction mixture was heated to 60° C. and stirred for 3 days. The DMF was removed in vacuo (1 mmHg, 60° C.) and to this crude material was added methylene chloride (5 mL), acetic anhydride (5 mmol, 0.47 mL) and triethylamine (5 mmol, 0.7 mL), and the mixture was stirred overnight. Silica gel flash chromatography using 10% methanol:methylene chloride gave an amber oil which was dissolved in methylene chloride (10 mL) and extracted with saturated sodium bicarbonate (2×20 mL), water (1×20 mL), saturated brine (1×20 mL) and dried over sodium sulfate. The solvent was removed in vacuo to give pure product (0.38 g, 15.3%); DCI/MS (M+1)= 498; 300 MHz 1H NMR (CDCl3)δ: 8.4(d,2H,J=1.25 Hz), 7.3 (m,4H), 7.2 (d,2H,J=1.4 Hz), 6.95 (m, 4H), 5.1 (m, 1H), 4.2 (s, 1H), 3.3 and 3.2 (d of d and d of d, 2H), 2.6 (d, 2H,J=6.1 Hz), 2.35 (m, 8H), 2.0 (s,3H).

後処理

  1. customThe DMF was removed in vacuo (1 mmHg, 60° C.) and to this crude material
  2. stirringthe mixture was stirred overnight
  3. extractionextracted with saturated sodium bicarbonate (2×20 mL), water (1×20 mL), saturated brine (1×20 mL)
  4. dry with materialdried over sodium sulfate
  5. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-8bf179eeca7a4f2fadb4200bd644a342
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05215987

反応ノート

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