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

Water → (4-(6,7-Bis(palmitoyloxy)-2-methyl-4-thiaheptanoyl)amino-benzoyl)glutamic acid di-t-butyl ester

HRID 1720836
ノート
印刷プレビュー

反応式

HRID 1720836 の反応式
[C:1]([O:5][C:6](=[O:27])[C@H:7]([CH2:18][CH2:19][C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[NH:8][C:9](=[O:17])[C:10]1[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1)([CH3:4])([CH3:3])[CH3:2].[C:28]([O:45][CH:46]([CH2:55][O:56][C:57](=[O:73])[CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][CH2:71][CH3:72])[CH2:47][S:48][CH2:49][CH:50]([CH3:54])[C:51](O)=[O:52])(=[O:44])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43].O>N1C=CC=CC=1.P(Cl)(Cl)Cl>[C:1]([O:5][C:6](=[O:27])[C@H:7]([CH2:18][CH2:19][C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[NH:8][C:9](=[O:17])[C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:51](=[O:52])[CH:50]([CH3:54])[CH2:49][S:48][CH2:47][CH:46]([O:45][C:28](=[O:44])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])[CH2:55][O:56][C:57](=[O:73])[CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][CH2:71][CH3:72])=[CH:12][CH:11]=1)([CH3:3])([CH3:4])[CH3:2]
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 962WaterHCID 105324766,7-Bis(palmitoyloxy)-2-methyl-4-thiaheptanoic acidHCID 10691066L-Glutamic acid, N-(4-aminobenzoyl)-, bis(1,1-dimethylethyl) ester

生成物 1

HCID 10701254(4-(6,7-Bis(palmitoyloxy)-2-methyl-4-thiaheptanoyl)amino-benzoyl)glutamic acid di-t-butyl ester収率 62%

試薬・触媒・溶媒 2

HCID 1049
Pyridine
溶媒
HCID 24387Phosphorus trichloride溶媒

実験手順

To a solution of 4-aminobenzoylglutamic acid di-t-butyl ester (378 mg) in pyridine (5 ml), phosphorus trichloride (0.044 ml) was added, followed by stirring at room temperature for 2 hours. To this solution, 6,7-bis(palmitoyloxy)-2-methyl-4-thiaheptanoic acid as obtained in Reference Example 42 (336 mg) was added, followed by stirring at room temperature for 24 hours. After addition of water, the reaction mixture was extracted with ethyl acetate. The extract was washed with a 5% aqueous solution of citric acid, a saturated aqueous solution of sodium hydrogen carbonate and saturated saline, and dried over anhydrous sodium sulfate, and the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate =2:1) to yield the title compound (315 mg, yield 62%) as a wax-like substance.

後処理

  1. additionwas added
  2. stirringby stirring at room temperature for 24 hours
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe extract was washed with a 5% aqueous solution of citric acid
  5. dry with materiala saturated aqueous solution of sodium hydrogen carbonate and saturated saline, and dried over anhydrous sodium sulfate
  6. distillationthe solvent was distilled off
  7. customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate =2:1)

出典と根拠

ORDレコード
ord-e8e5ecff5b0c448c8aa628bf484d181f
出典データセット
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05506267

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