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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2,6-Diaminopyridine-3-carboxamide

HRID 1927227
ノート
印刷プレビュー

反応式

HRID 1927227 の反応式
[NH2:1][C:2]1[N:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].CC[N:14]=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.[Cl-].[NH4+].C(N(C(C)C)CC)(C)C>O.CS(C)=O>[NH2:1][C:2]1[N:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:3]=1[C:4]([NH2:14])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 25517Ammonium ChlorideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 189772452,6-Diaminonicotinic acid

生成物 1

HCID 204748872,6-Diaminopyridine-3-carboxamide収率 73.8%

試薬・触媒・溶媒

2
HCID 679Dimethyl Sulfoxide溶媒HCID 962Water溶媒

実験手順

2,6-Diaminonicotinic acid (1.5 g), WSC (2.8 g), HOBt (2.0 g), ammonium chloride (1.6 g), diisopropylethylamine (7.6 g), and DMSO (45 mL) were stirred for 15 hours at room temperature. Water was added to the reaction solution, which was then extracted with ethyl acetate. The organic layer was concentrated and purified by silica gel chromatography (ethyl acetate, then ethyl acetate:methanol=4:1). The organic layer thus obtained was concentrated and purified by NH silica gel column chromatography (ethyl acetate). Ethyl acetate and hexane were added to the residue thus obtained, and the solids were filtered off to obtain the titled compound (1.1 g).

後処理

  1. extractionwas then extracted with ethyl acetate
  2. concentrationThe organic layer was concentrated
  3. custompurified by silica gel chromatography (ethyl acetate
  4. customThe organic layer thus obtained
  5. concentrationwas concentrated
  6. custompurified by NH silica gel column chromatography (ethyl acetate)
  7. additionEthyl acetate and hexane were added to the residue
  8. customthus obtained
  9. filtrationthe solids were filtered off

出典と根拠

ORDレコード
ord-01050031bd7d42c6ae7a0e2674aca124
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183264B2

反応ノート

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