Benzylamine → 4-Ethyl-5-(4-methylbenzylamino)-2-t-butyl-3(2H)pyridazinone

HRID 2372342노트

반응식

HRID 2372342 반응식
[CH2:1]([C:3]1[C:4](=[O:14])[N:5]([C:10]([CH3:13])([CH3:12])[CH3:11])[N:6]=[CH:7][C:8]=1Cl)[CH3:2].C(N)C1C=CC=CC=1.[CH3:23][C:24]1[CH:31]=[CH:30][C:27]([CH2:28][NH2:29])=[CH:26][CH:25]=1>>[CH2:1]([C:3]1[C:4](=[O:14])[N:5]([C:10]([CH3:13])([CH3:12])[CH3:11])[N:6]=[CH:7][C:8]=1[NH:29][CH2:28][C:27]1[CH:30]=[CH:31][C:24]([CH3:23])=[CH:25][CH:26]=1)[CH3:2]

참가 물질

4

반응물 3

HCID 7504BenzylamineHCID 660354-MethylbenzylamineHCID 138250102-t-butyl-5-chloro-4-ethyl-3(2H)-pyridazinone

생성물 1

HCID 138538904-Ethyl-5-(4-methylbenzylamino)-2-t-butyl-3(2H)pyridazinone

실험 절차

The compound as identified in Table 14 was prepared in the synthetic manner and after-treatment similar to those in Example 7 except that the 4-alkyl-5-chloro-2-alkyl-3(2H)pyridazinone with R1 and R2 as identified in Table 14 was used instead of the starting 4-ethyl-5-chloro-2-t-butyl-3(2H)pyridazinone used in Example 7, and the benzylamine derivative with R3, Y1, Y2 and Y3 as identified in Table 14 was used instead of the starting 4-methylbenzylamine. In the NMR data, only the characteristic absorptions were given in Table 14.

후처리

  1. customwas prepared in the synthetic manner

출처 및 근거

ORD 기록
ord-a1bcb333fa1f4485af4f9c67115e435f
출처 데이터셋
uspto-grants-1992_03
특허 번호
US05098900

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