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 → 2-((3-(7-Bromo-1-carbamoyl-9H-pyrido[3,4-b]indol-4-yl)-2-methylphenylamino)methyl)-5-methoxybenzoic acid

HRID 2361368
ノート
印刷プレビュー

反応式

HRID 2361368 の反応式
[NH2:1][C:2]1[C:3]([CH3:25])=[C:4]([C:8]2[C:20]3[C:19]4[C:14](=[CH:15][C:16]([Br:21])=[CH:17][CH:18]=4)[NH:13][C:12]=3[C:11]([C:22]([NH2:24])=[O:23])=[N:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[CH:26]([C:28]1[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][C:29]=1[C:30]([OH:32])=[O:31])=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(O)(=O)C>ClCCl.O1CCCC1>[Br:21][C:16]1[CH:15]=[C:14]2[C:19]([C:20]3[C:8]([C:4]4[C:3]([CH3:25])=[C:2]([NH:1][CH2:26][C:28]5[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][C:29]=5[C:30]([OH:32])=[O:31])[CH:7]=[CH:6][CH:5]=4)=[CH:9][N:10]=[C:11]([C:22](=[O:23])[NH2:24])[C:12]=3[NH:13]2)=[CH:18][CH:17]=1
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 176Acetic AcidHCID 5049666Sodium triacetoxyborohydrideHCID 71762052-Formyl-5-methoxybenzoic acidHCID 679947214-(3-amino-2-methylphenyl)-7-bromo-9H-pyrido[3,4-b]indole-1-carboxamide

生成物 1

HCID 679947572-((3-(7-Bromo-1-carbamoyl-9H-pyrido[3,4-b]indol-4-yl)-2-methylphenylamino)methyl)-5-methoxybenzoic acid収率 163.1%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of 4-(3-amino-2-methylphenyl)-7-bromo-9H-pyrido[3,4-b]indole-1-carboxamide (0.184 g, 0.466 mmol), 2-formyl-5-methoxybenzoic acid (0.210 g, 1.164 mmol), sodium triacetoxyborohydride (0.296 g, 1.397 mmol), and acetic acid (0.067 mL, 1.164 mmol) in dichloromethane (14 mL) and tetrahydrofuran (14 mL) was stirred at room temperature for 16 hr. The reaction was quenched with water (30 mL) and the mixture was extracted with ethyl acetate (3×40 mL). The combined extract was washed with brine (30 ml) and dried over anhydrous MgSO4. Removal of solvent under vacuum provided the crude desired product (0.425 g, 0.760 mmol, 163% yield) as a beige solid. The crude product was used in the next step without further purification.

後処理

  1. customThe reaction was quenched with water (30 mL)
  2. extractionthe mixture was extracted with ethyl acetate (3×40 mL)
  3. extractionThe combined extract
  4. washwas washed with brine (30 ml)
  5. dry with materialdried over anhydrous MgSO4
  6. customRemoval of solvent under vacuum

出典と根拠

ORDレコード
ord-e90dc2631de545a880baed1c836e1449
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08685969B2

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