Hydrazine hydrate (1:1) → HCID 178452030、化合物

HRID 1476903ノート

反応式

HRID 1476903 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([NH:12][C@H:13]1[CH2:17][CH2:16][N:15]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:14]1)=[N:9][C:8]([C:25]#[N:26])=[CH:7]2.[NH2:27][NH2:28].O>CO>[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([NH:12][C@H:13]1[CH2:17][CH2:16][N:15]([C:18]([O:20][C:21]([CH3:23])([CH3:22])[CH3:24])=[O:19])[CH2:14]1)=[N:9][C:8]([C:25]([NH:27][NH2:28])=[NH:26])=[CH:7]2

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 90387268(S)-tert-butyl 3-((8-chloro-3-cyanoisoquinolin-1-yl)amino)pyrrolidine-1-carboxylate

生成物 1

HCID 178452030HCID 178452030、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a mixture of (S)-tert-butyl 3-((8-chloro-3-cyanoisoquinolin-1-yl)amino)pyrrolidine-1-carboxylate (450 mg, 1.21 mmol) in MeOH (5 mL) was added NH2NH2—H2O (5 mL). The resulting mixture was heated to reflux for 2 hours and the solvent was subsequently removed to give the title compound as a yellow solid, which was used without further purification (450 mg, 91%). ESI-MS m/z [M+H]+ 405.2.

後処理

  1. temperatureThe resulting mixture was heated
  2. temperatureto reflux for 2 hours
  3. customthe solvent was subsequently removed

出典と根拠

ORDレコード
ord-6114900e6aa840be866b797d57b2ae93
出典データセット
uspto-grants-2016_08
特許番号
US09402841B2

反応ノート

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