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Hydrochloric Acid → 4-Chloropyridin-2-amine--hydrogen chloride (1/1)

HRID 1696196
ノート
印刷プレビュー

反応式

HRID 1696196 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4](C(O)=O)[CH:3]=1.C([N:13](CC)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.Cl>C(O)(C)(C)C.O1CCOCC1.O>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH2:13])[CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 2308904-Chloropyridine-2-carboxylic acid

生成物 1

HCID 533020304-Chloropyridin-2-amine--hydrogen chloride (1/1)

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 6386
tert-Butanol
溶媒
HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
100 °C

実験手順

To a solution of 4-chloro-2-pyridinecarboxylic acid (5.95 g) in tert-butanol (89.25 mL) were added triethylamine (6.32 mL) and diphenylphosphoryl azide (8.95 mL). The mixture was stirred at 100° C. for overnight. To the solution was added water and the mixture was extracted with EtOAc and washed with water and brine. The extract was dried over MgSO4 and concentrated under reduced pressure. The residue was recrystallized with EtOAc to give a white solid. The solid was dissolved in dioxane (50 mL). To the solution was added 4M HCl in dioxane (90 mL) and the mixture was stirred at ambient temperature overnight. The mixture was concentrated under reduced pressure to give 4-chloro-2-pyridinamine hydrochloride (3.02 g) as a white solid.

後処理

  1. extractionthe mixture was extracted with EtOAc
  2. washwashed with water and brine
  3. dry with materialThe extract was dried over MgSO4
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was recrystallized with EtOAc
  6. customto give a white solid
  7. stirringthe mixture was stirred at ambient temperature overnight
  8. concentrationThe mixture was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-b30eb359faba4260b8476a08651b3750
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163767B2

反応ノート

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