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

Methyl 4-chloroanthranilate → HCID 11754542、化合物

HRID 225772
ノート
印刷プレビュー

反応式

HRID 225772 の反応式
CO[C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:5]=1[NH2:11].C1CN([P+](Br)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C.CO[C:48](=O)[C:49]1[CH:54]=[CH:53][C:52](Cl)=[CH:51][C:50]=1[NH:56][C:57]([CH:59]1[CH2:64][CH2:63][CH2:62][CH2:61][N:60]1[C:65](=[O:73])[C:66]1[CH:71]=[CH:70][C:69]([CH3:72])=[CH:68][CH:67]=1)=O>CN(C=O)C>[CH2:50]([N:56]1[C:3](=[O:12])[C:4]2[C:5](=[CH:6][C:7]([Cl:10])=[CH:8][CH:9]=2)[N:11]=[C:57]1[CH:59]1[CH2:64][CH2:63][CH2:62][CH2:61][N:60]1[C:65](=[O:73])[C:66]1[CH:71]=[CH:70][C:69]([CH3:72])=[CH:68][CH:67]=1)[C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:48]=1
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 4

HCID 80001Methyl 4-chloroanthranilateHCID 81531DiisopropylethylamineHCID 2733179PyBroPHCID 69063202HCID 69063202、化合物

生成物 1

HCID 11754542HCID 11754542、化合物収率 21%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

In an ice bath at −15° C., pure compound of Formula 202 (7.2 g, 29 mmol) was combined with 2-amino-4-chloro-benzoic acid methyl ester (4.5 g, 24 mmol), PyBroP (2.3 g, 4.9 mmol) and diisopropylethylamine (0.95 mL, 5.4 mmol) in DMF (30 mL). The resulting mixture was stirred ovemight, allowing the temperature to rise to room temperature with the bath. The solution was concentrated under vacuum and the residue partitioned between ethyl acetate (200 mL) and water (200 mL). The organic layer was washed with water (3×100 mL) and concentrated under vacuum. The resulting residue was purified by silica gel chromatography using 40% ethyl acetate/hexanes as eluent to give 2.66 g (21% yield) of the desired product of Formula 203, 4-chloro-2-{[1-(4-methyl-benzoyl)-piperidine-2-carbonyl]amino}-benzoic acid methyl ester, as a crystalline solid. LRMS (MH+) m/z 472.

後処理

  1. customto rise to room temperature with the bath
  2. concentrationThe solution was concentrated under vacuum
  3. customthe residue partitioned between ethyl acetate (200 mL) and water (200 mL)
  4. washThe organic layer was washed with water (3×100 mL)
  5. concentrationconcentrated under vacuum
  6. customThe resulting residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-54f87a778ce448d29bfe294692fd351c
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07557115B2

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