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Picolinic acid → HCID 66803437、化合物

HRID 341429
ノート
印刷プレビュー

反応式

HRID 341429 の反応式
C(N(CC)CC)C.N1(O)C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[N:30]1[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=1[C:36]([OH:38])=O.[NH2:39][C:40]1[N:45]=[C:44]([NH:46][C:47]2[CH:52]=[CH:51][CH:50]=[C:49]([Cl:53])[C:48]=2[F:54])[N:43]=[C:42]([C:55](=[N:57]O)[NH2:56])[N:41]=1>CN(C=O)C>[Cl:53][C:49]1[C:48]([F:54])=[C:47]([NH:46][C:44]2[N:45]=[C:40]([NH2:39])[N:41]=[C:42]([C:55]3[N:56]=[C:36]([C:31]4[CH:32]=[CH:33][CH:34]=[CH:35][N:30]=4)[O:38][N:57]=3)[N:43]=2)[CH:52]=[CH:51][CH:50]=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 5

HCID 1018Picolinic acidHCID 8471TriethylamineHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 136377136HCID 136377136、化合物

生成物 1

HCID 66803437HCID 66803437、化合物収率 17%

試薬・触媒・溶媒

1
HCID 6228Dimethylformamide溶媒

実験手順

Triethylamine (1.10 mL, 7.58 mmol) and 1H-benzotriazol-1-ol (0.77 g, 5.05 mmol) were added to a solution of N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (0.97 g, 5.05 mmol) in DMF (10 mL) and the mixture was stirred for 20 min at room temperature. Picolinic acid (0.62 g, 5.05 mmol) was added and the mixture was stirred for 30 min at room temperature. 4-Amino-6-[(3-chloro-2-fluorophenyl)amino]-N′-hydroxy-1,3,5-triazine-2-carboximidamide (prepared in an analogous manner to Intermediate 73, 1.50 g, 5.05 mmol) was added and the mixture was stirred at room temperature overnight before being heated to 85 C for approximately 24 h. The crude compound was purified over Ambersep resin but the impurities remained. The residue was then successively washed with EtOAc, acetone and MeOH and finally hot MeOH to afford the title compound (330 mg, 17%).

後処理

  1. stirringthe mixture was stirred for 30 min at room temperature
  2. additionwas added
  3. stirringthe mixture was stirred at room temperature overnight
  4. temperaturebefore being heated to 85 C for approximately 24 h
  5. customThe crude compound was purified over Ambersep resin
  6. washThe residue was then successively washed with EtOAc, acetone and MeOH and finally hot MeOH

出典と根拠

ORDレコード
ord-f924023dc9be4756ba4aedddc1759c9b
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895733B2

反応ノート

読み込み中…

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