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

Triethylamine → HCID 86665014、化合物

HRID 244378
ノート
印刷プレビュー

反応式

HRID 244378 の反応式
[CH2:1]([N:8]([CH2:46][C:47]1[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=1)[CH2:9][CH2:10][N:11]1[C:16]2[CH:17]=[C:18]([C:22](=[O:40])[N:23]([C@@H:27]3[CH2:32][CH2:31][CH2:30][N:29]([C:33]([O:35][C:36]([CH3:39])([CH3:38])[CH3:37])=[O:34])[CH2:28]3)[CH:24]([CH3:26])[CH3:25])[C:19]([CH3:21])=[CH:20][C:15]=2[O:14][C:13]([CH3:44])([C:41](O)=[O:42])[C:12]1=[O:45])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.C(OC(Cl)=O)C(C)C>O1CCCC1>[CH2:1]([N:8]([CH2:46][C:47]1[CH:48]=[CH:49][CH:50]=[CH:51][CH:52]=1)[CH2:9][CH2:10][N:11]1[C:16]2[CH:17]=[C:18]([C:22]([N:23]([CH:24]([CH3:25])[CH3:26])[C@@H:27]3[CH2:32][CH2:31][CH2:30][N:29]([C:33]([O:35][C:36]([CH3:38])([CH3:39])[CH3:37])=[O:34])[CH2:28]3)=[O:40])[C:19]([CH3:21])=[CH:20][C:15]=2[O:14][C:13]([CH2:41][OH:42])([CH3:44])[C:12]1=[O:45])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 62365Isobutyl chloroformateHCID 67512141HCID 67512141、化合物

生成物 1

HCID 86665014HCID 86665014、化合物収率 84.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Under nitrogen atmosphere, the mixture was cooled with ice-bath, and to a solution of the obtained 4-[2-(dibenzylamino)ethyl]-2,7-dimethyl-6-{[(3R)-1-{[(2-methyl-2-propanyl)oxy]carbonyl}-3-piperidinyl](2-propanyl)carbamoyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylic acid (27.2 g) in tetrahydrofuran (75 ml) were added triethylamine (5.8 g) and chloroformic acid isobutyl ester (6.2 g), and the mixture was stirred for one hour. The precipitated salt was filtered, and the filtrate was added dropwise into a suspension of sodium borohydride (2.9 g) in tetrahydrofuran-ethanol (50 ml-50 ml) under ice-cooling. The mixture was stirred for one hour, and thereto was added a saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, and dried over sodium sulfate. The sodium sulfate was removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography to give 2-methyl-2-propanyl (3R)-3-[({4-[2-(dibenzylamino)ethyl]-2-(hydroxymethyl)-2,7-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl}carbonyl)(2-propanyl)amino]-1-piperidinecarboxylate (22.5 g).

後処理

  1. temperatureUnder nitrogen atmosphere, the mixture was cooled with ice-bath
  2. filtrationThe precipitated salt was filtered
  3. additionthe filtrate was added dropwise into a suspension of sodium borohydride (2.9 g) in tetrahydrofuran-ethanol (50 ml-50 ml) under ice-
  4. temperaturecooling
  5. stirringThe mixture was stirred for one hour
  6. additionwas added a saturated aqueous ammonium chloride solution
  7. extractionthe mixture was extracted with ethyl acetate
  8. washThe organic layer was washed with a saturated aqueous sodium chloride solution
  9. dry with materialdried over sodium sulfate
  10. customThe sodium sulfate was removed by filtration
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. customThe obtained residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-ca8101e570754a089586a3bf8ffb9eee
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658639B2

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