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Ammonia methanol → 2-(5-chloro-2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)ethanamine

HRID 887795
ノート
印刷プレビュー

反応式

HRID 887795 の反応式
[Cl:1][C:2]1[C:3]2[CH2:14][CH2:13][C:12](=[CH:15][C:16]#[N:17])[C:4]=2[C:5]2[C:9]([CH:10]=1)=[N:8][N:7]([CH3:11])[CH:6]=2.N.CO>CO.O1CCCC1.[Co]>[Cl:1][C:2]1[C:3]2[CH2:14][CH2:13][C:12](=[CH:15][CH2:16][NH2:17])[C:4]=2[C:5]2[C:9]([CH:10]=1)=[N:8][N:7]([CH3:11])[CH:6]=2
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 21705897Ammonia methanolHCID 68697773(5-chloro-2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)acetonitrile

生成物 1

HCID 686990322-(5-chloro-2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)ethanamine収率 100%

試薬・触媒・溶媒 3

HCID 104730Cobalt触媒HCID 887Methanol溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

(5-Chloro-2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)acetonitrile (116 mg, 2.87 mmol) was dissolved in a mixture of methanol (5 mL) and tetrahydrofuran (5 mL), Raney cobalt (1 g) and 8M ammonia/methanol solution (2 mL) were added to the solution, and the mixture was stirred under a hydrogen atmosphere at room temperature for 4 hr. The catalyst was filtered off through celite, and the filtrate was concentrated under reduced pressure to give the title compound (118 mg, yield 100%).

後処理

  1. additionwere added to the solution
  2. filtrationThe catalyst was filtered off through celite
  3. concentrationthe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-140a997a8c8e4444ade85b276248a7df
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08247429B2

反応ノート

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