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

Lithium Hydroxide → HCID 44818729、化合物

HRID 1951642
ノート
印刷プレビュー

反応式

HRID 1951642 の反応式
[CH3:1][C:2]1[S:9][C:8]2[CH:7]=[CH:6][N:5]([CH2:10][C:11]3[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=3)[C:4]=2[C:3]=1[C:21](O)=[O:22].C[O:25][C:26](=[O:36])[C:27]1[CH:32]=[CH:31][C:30]([C@@H:33]([NH2:35])[CH3:34])=[CH:29][CH:28]=1.Cl.C(N=C=NCCCN(C)C)C.CN1CCOCC1.[Li+].[OH-]>CN(C=O)C.C1COCC1.O.CO>[CH3:1][C:2]1[S:9][C:8]2[CH:7]=[CH:6][N:5]([CH2:10][C:11]3[CH:12]=[CH:13][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:15][CH:16]=3)[C:4]=2[C:3]=1[C:21]([NH:35][C@H:33]([C:30]1[CH:31]=[CH:32][C:27]([C:26]([OH:25])=[O:36])=[CH:28][CH:29]=1)[CH3:34])=[O:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 5

HCID 3939Lithium HydroxideHCID 79724-MethylmorpholineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 17751895Methyl 4-((1S)-1-aminoethyl)benzoateHCID 671826242-Methyl-4-(4-(trifluoromethyl)benzyl)-4H-thieno[3,2-b]pyrrole-3-carboxylic acid

生成物 1

HCID 44818729
HCID 44818729、化合物
収率 47%

試薬・触媒・溶媒 4

HCID 887Methanol溶媒HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of 0.043 g of 2-methyl-4-(4-trifluoromethyl-benzyl)-4H-thieno[3,2-b]pyrrole-3-carboxylic acid, 0.060 g of (S)-4-(1-amino-ethyl)-benzoic acid methyl ester, 0.040 g of HOBT-hydrate, 0.054 g of ethyl-dimethylaminopropyl-carbodiimide hydrochloride (EDCI) and 0.060 ml of N-methylmorpholine in 2 ml of DMF was stirred at room temperature for 18 h. The reaction was then quenched with 1 ml of water and 2 ml of saturated NaHCO3 solution. The resulting mixture extracted with 15 ml of EtOAc. The organic layer was dried over Na2SO4, filtered, and concentrated to give the crude methyl ester which was dissolved in 2 ml THF, 2 mL MeOH and 0.5 mL water and treated with 0.5 mL of 1M LiOH solution. After stirring for 24 h at room temperature, the reaction mixture was concentrated under reduced pressure to remove THF and MeOH. The residue was diluted with 2 mL of water and treated with 0.3 mL of AcOH with vigorous stirring. After stirring for 2 h, the solid was collected by filtration and air-dried to give 0.029 g of the title compound as a white powder.

後処理

  1. customThe reaction was then quenched with 1 ml of water and 2 ml of saturated NaHCO3 solution
  2. extractionThe resulting mixture extracted with 15 ml of EtOAc
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customto give the crude methyl ester which
  7. stirringAfter stirring for 24 h at room temperature
  8. concentrationthe reaction mixture was concentrated under reduced pressure
  9. customto remove THF and MeOH
  10. additionThe residue was diluted with 2 mL of water
  11. additiontreated with 0.3 mL of AcOH with vigorous stirring
  12. stirringAfter stirring for 2 h
  13. filtrationthe solid was collected by filtration
  14. customair-dried

出典と根拠

ORDレコード
ord-d4a17d1c805a4cbfa9afabf65f2dc547
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08404736B2

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