反応 #1107

ord-61a0177588e440db829d21a8578b91c1

反応方程式

COc1c(Nc2ccc(C(C)(C)C)cc2)ccnc1C
4-(4-tert-butylanilino)-3-methoxy-2-methylpyridine
COc1c(NC2CCC(C(C)(C)C)CC2)ccnc1C
4-(4-tert-Butylcyclohexylamino)-3-methoxy-2-methylpyridine

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他are hydrogenated at room temperature
  2. 2
    その他normal pressure until absorption of hydrogen
  3. 3
    ろ過After filtering
  4. 4
    濃縮concentrating 1 g of syrup

実験手順

1 g of 4-(4-tert-butylanilino)-3-methoxy-2-methylpyridine in 20 ml of methanol, 3.7 ml of 2N HCl and 1.3 ml of water are hydrogenated at room temperature and normal pressure until absorption of hydrogen has ended using 1 g of rhodium on alumina (5% strength). After filtering and concentrating 1 g of syrup remains=100% isomer mixture.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723450uspto-grants-1998_03