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

2-(Adamantan-1-yl)-N-methylethan-1-amine → HCID 21974209、化合物

HRID 2075907
ノート
印刷プレビュー

反応式

HRID 2075907 の反応式
ClC(Cl)(O[C:5](=[O:11])OC(Cl)(Cl)Cl)Cl.[C:13]12([CH2:23][CH2:24][NH:25][CH3:26])[CH2:22][CH:17]3[CH2:18][CH:19]([CH2:21][CH:15]([CH2:16]3)[CH2:14]1)[CH2:20]2.C(N(C(C)C)CC)(C)C.[CH3:36][NH:37][CH2:38][CH2:39][CH2:40][C:41]1[CH:46]=[CH:45][N:44]=[CH:43][CH:42]=1>ClCCl.C(OCC)C>[C:13]12([CH2:23][CH2:24][N:25]([CH3:26])[C:5]([N:37]([CH3:36])[CH2:38][CH2:39][CH2:40][C:41]3[CH:42]=[CH:43][N:44]=[CH:45][CH:46]=3)=[O:11])[CH2:20][CH:19]3[CH2:18][CH:17]([CH2:16][CH:15]([CH2:21]3)[CH2:14]1)[CH2:22]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 4

HCID 359962-(Adamantan-1-yl)-N-methylethan-1-amineHCID 81531Diisopropylethylamine2 回HCID 94429TriphosgeneHCID 21974070N-Methyl-3-(pyridin-4-yl)propan-1-amine

生成物 1

HCID 21974209HCID 21974209、化合物収率 141.6%

試薬・触媒・溶媒 2

HCID 3283
Diethyl Ether
溶媒
HCID 6344Dichloromethane溶媒3 回

実験手順

A solution of triphosgene (190 mg, 0.640 mmol) in dichloromethane (6.0 ml) was stirred at room temperature under a nitrogen atmosphere. A solution of 2-(1-adamantyl)-N-methylethylamine (Intermediate No. 3-1) (330 mg, 1.71 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dichloromethane (6.0 ml) was added dropwise thereto over 17 minutes. After eight minutes, a solution of N-methyl-3-(4-pyridyl)propylamine (Intermediate No. 3-3) (264 mg, 1.78 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dichloromethane (5.1 ml) was added to the mixture at a stretch, and the whole was stirred for 20 hours. The reaction mixture was diluted with diethyl ether (40 ml), the whole was washed with a saturated aqueous sodium hydrogencarbonate solution (40 ml) twice and a saturated aqueous sodium chloride solution (40 ml) successively, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give 335 mg (54%) of the titled compound.

後処理

  1. waitAfter eight minutes
  2. washthe whole was washed with a saturated aqueous sodium hydrogencarbonate solution (40 ml) twice
  3. dry with materiala saturated aqueous sodium chloride solution (40 ml) successively, and the organic layer was dried over magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-b74c24f4aee8402686e3d33d80ff1ca1
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07923461B2

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