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

Potassium Carbonate → (R)-tert-Butyl 1-methoxy-3-(3-oxo-4-(m-tolylamino)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)propan-2-ylcarbamate

HRID 516082
ノート
印刷プレビュー

反応式

HRID 516082 の反応式
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:32][O:33][CH3:34])[CH2:10][NH:11][C:12]1[CH:21]=[C:20]([C:22]#[N:23])[C:15]([C:16]([O:18]C)=O)=[C:14]([NH:24][C:25]2[CH:26]=[C:27]([CH3:31])[CH:28]=[CH:29][CH:30]=2)[N:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>C(O)(=O)C.C(Cl)Cl.[Pt](=O)=O>[CH3:34][O:33][CH2:32][C@H:9]([NH:8][C:6](=[O:7])[O:5][C:1]([CH3:3])([CH3:2])[CH3:4])[CH2:10][NH:11][C:12]1[N:13]=[C:14]([NH:24][C:25]2[CH:26]=[C:27]([CH3:31])[CH:28]=[CH:29][CH:30]=2)[C:15]2[C:16](=[O:18])[NH:23][CH2:22][C:20]=2[CH:21]=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 2

HCID 11430Potassium CarbonateHCID 67238996(R)-Methyl 6-(2-(tert-butoxycarbonylamino)-3-methoxypropylamino)-4-cyano-2-(m-tolylamino)nicotinate

生成物 1

HCID 67238901(R)-tert-Butyl 1-methoxy-3-(3-oxo-4-(m-tolylamino)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)propan-2-ylcarbamate

試薬・触媒・溶媒 3

HCID 345198Adams' catalyst触媒HCID 176
Acetic Acid
溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

To a round-bottomed flask was added (R)-methyl 6-(2-(tert-butoxycarbonylamino)-3-methoxypropylamino)-4-cyano-2-(m-tolylamino)nicotinate (84.5 mg, 0.180 mmol) in acetic acid (3 mL) and DCM (10 mL). To the resulting yellow solution was added platinum(IV) oxide (4.09 mg, 0.018 mmol). The flask was evacuated and back filled with hydrogen (3×1 atm). The reaction mixture was stirred vigorously at RT for 16 h, subsequently diluted with DCM (10 mL), and filtered through Celite. The filtrate was concentrated to an oil, which was diluted with DCM (10 mL). Potassium carbonate (24.87 mg, 0.180 mmol) was added and the reaction mixture was stirred at RT for 12 h. The crude reaction was diluted with DCM (10 mL), filtered through Celite, and concentrated to give the title compound as a thick yellow oil, which was used without further purification (26.5 mg, 33.4%). [M+H] calc'd for C23H31N5O4, 442; found, 442.

後処理

  1. customThe flask was evacuated
  2. additionback filled with hydrogen (3×1 atm)
  3. additionsubsequently diluted with DCM (10 mL)
  4. filtrationfiltered through Celite
  5. concentrationThe filtrate was concentrated to an oil, which
  6. additionwas diluted with DCM (10 mL)
  7. stirringthe reaction mixture was stirred at RT for 12 h
  8. customThe crude reaction
  9. filtrationfiltered through Celite
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-6354ce374ba74d49bd72ea0a1d405c23
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09108970B2

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