Water → HCID 57069684、化合物

HRID 2231977ノート

反応式

HRID 2231977 の反応式
[Cl:1][C:2]1[N:9]=[C:8](Cl)[CH:7]=[C:6]([CH3:11])[C:3]=1[C:4]#[N:5].NCCNC(=O)[CH:17]([C:19]1[CH:24]=[C:23]([C:25]([CH3:28])([CH3:27])[CH3:26])[C:22]([OH:29])=[C:21]([C:30]([CH3:33])([CH3:32])[CH3:31])[CH:20]=1)[CH3:18].C([N:37](CC)CC)C.O.C[N:44]1[CH2:48][CH2:47]C[C:45]1=[O:49]>C1(C)C=CC=CC=1>[C:30]([C:21]1[CH:20]=[C:19]([CH2:17][CH2:18][C:45]([NH:44][CH2:48][CH2:47][NH:37][C:8]2[CH:7]=[C:6]([CH3:11])[C:3]([C:4]#[N:5])=[C:2]([Cl:1])[N:9]=2)=[O:49])[CH:24]=[C:23]([C:25]([CH3:28])([CH3:26])[CH3:27])[C:22]=1[OH:29])([CH3:33])([CH3:32])[CH3:31]

参加物

7

実験手順

18.7 g of 2,6-dichloro-4-methylnicotinonitrile and 32 g of 3,5-di-tert-butyl-4-hydroxyphenylpropionic acid 2-aminoethylamide are reacted with 10.1 g of triethylamine in 0.2 l of N-methylpyrrolidone at 50° C. for 8 hours, after which 1 l of water and 0.4 l of toluene are added, the toluene phase is separated off, dried and filtered over active carbon, and the filtrate is evaporated down. The residue is dissolved in 100 ml of hot ethanol, and 1 l of petroleum ether is slowly added to the solution. The mixture is cooled, and the precipitate is filtered off under suction and dried to give a product of melting point 162°-165° C.

後処理

  1. customthe toluene phase is separated off
  2. customdried
  3. filtrationfiltered over active carbon
  4. customthe filtrate is evaporated down
  5. dissolutionThe residue is dissolved in 100 ml of hot ethanol
  6. addition1 l of petroleum ether is slowly added to the solution
  7. temperatureThe mixture is cooled
  8. filtrationthe precipitate is filtered off under suction
  9. customdried
  10. customto give a product of melting point 162°-165° C.

出典と根拠

ORDレコード
ord-23c2844a1e964804a3e1820609c83d29
出典データセット
uspto-grants-1988_11
特許番号
US04785107

反応ノート

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