3-Pyridinemethanamine → Pyrinuron

HRID 616698

反応式

HRID 616698 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]=[C:11]=[O:12])=[CH:6][CH:5]=1)([O-:3])=[O:2].[NH2:13][CH2:14][C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1>C1(C)C=CC=CC=1>[N:17]1[CH:18]=[CH:19][CH:20]=[C:15]([CH2:14][NH:13][C:11]([NH:10][C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)=[O:12])[CH:16]=1

参加物

4

反応物 2

HCID 310183-PyridinemethanamineHCID 66012Benzene, 1-isocyanato-4-nitro-2 回

生成物 1

HCID 40813Pyrinuron収率 98%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A solution of 415 g. of crude p-nitrophenyl isocyanate in 4.5 l. of toluene was stirred at room temperature. The mixture was filtered and 35 g. of insoluble impurity removed. The material in solution was 380 g. (2.32 mol) of purified p-nitrophenyl isocyanate. The solution was stirred under dry nitrogen, and 3-(aminomethyl)pyridine (250 g., 2.32 mol) was added dropwise. An exotherm to 40° C. was noted. The resulting thick suspension was stirred overnight and then vacuum filtered. The product was washed with hexane and dried in a vacuum oven at 60° C. overnight to give 610.7 g. melting at 220°-221.5° C. The product was a 98% yield of 1-(3-pyridylmethyl)-3-(4-nitrophenyl)urea. This product after recrystallization from 2-methoxyethanol melted with decomposition at 223°-225° C.

後処理

  1. filtrationThe mixture was filtered
  2. customof insoluble impurity removed
  3. customto 40° C.
  4. stirringThe resulting thick suspension was stirred overnight
  5. filtrationvacuum filtered
  6. washThe product was washed with hexane
  7. customdried in a vacuum oven at 60° C. overnight
  8. customto give 610.7 g

出典と根拠

ORDレコード
ord-967f7c487f354697afb83b170ba3ffbc
出典データセット
uspto-grants-1978_02
特許番号
US04075345

関連ノート

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