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

Acetic Acid → [4-(5-Chloro-isoquinolin-6-yloxy)-cyclohexyl]-cyclohexyl-amine

HRID 2370737
ノート
印刷プレビュー

反応式

HRID 2370737 の反応式
[Cl:1][C:2]1[C:11]([O:12][CH:13]2[CH2:18][CH2:17][C:16](=O)[CH2:15][CH2:14]2)=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][N:6]=[CH:7]2.C(N(CC)CC)C.[CH:27]1([NH2:33])[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1.C(O)(=O)C.C([BH3-])#N.[Na+]>CO>[Cl:1][C:2]1[C:11]([O:12][CH:13]2[CH2:18][CH2:17][CH:16]([NH:33][CH:27]3[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]3)[CH2:15][CH2:14]2)=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][N:6]=[CH:7]2
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 176Acetic AcidHCID 7965CyclohexylamineHCID 8471TriethylamineHCID 5003444Sodium cyanoborohydrideHCID 592685134-(5-Chloro-isoquinolin-6-yloxy)-cyclohexanone

生成物 1

HCID 25055878[4-(5-Chloro-isoquinolin-6-yloxy)-cyclohexyl]-cyclohexyl-amine収率 53.4%

試薬・触媒・溶媒

1
HCID 887Methanol溶媒2 回

実験手順

100 mg (0.36 mmol) 4-(5-Chloro-isoquinolin-6-yloxy)-cyclohexanone (79) were dissolved in 10 ml methanol. After adding 73 mg (0.73 mmol) triethyl amine, 108 mg (1.09 mmol) cyclohexylamine, 218 mg (3.63 mmol) acetic acid and freshly dried molecular sieves, the reaction was stirred at room temperature. After 30 minutes, a solution of 68 mg (1.09 mmol) sodium cyanoborohydride in 2 ml methanol was added and the reaction was kept at room temperature until complete conversion was achieved. For working up, the reaction mixture was filtered and the filtrate was brought to alkaline pH by adding solid NaHCO3. After evaporation of the solvent, the residue was taken up in H2O and extracted three times with dichloromethane. The combined organic layers were dried over MgSO4 and evaporated. Final purification by preparative HPLC gave 69 mg of the desired product as trifluoroacetate, which was dissolved in 2 N HCl and lyophilized, to yield 45 mg of the corresponding HCl-salt. Rt=1.08/1.15 min (Method #1). Detected mass: 359.3/361.3 (M+H+).

後処理

  1. customwas kept at room temperature until complete conversion
  2. filtrationthe reaction mixture was filtered
  3. additionby adding solid NaHCO3
  4. customAfter evaporation of the solvent
  5. extractionextracted three times with dichloromethane
  6. dry with materialThe combined organic layers were dried over MgSO4
  7. customevaporated
  8. customFinal purification by preparative HPLC

出典と根拠

ORDレコード
ord-de6808444b6545f08031604e66d1b1d7
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08710228B2

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