1,2,3-Trichloro-1-propene → HCID 54116225, compound

HRID 1107789

Reaction equation

HRID 1107789 reaction equation
[CH2:1]([O:8][C:9]1[N:10]=[N:11][CH:12]=[C:13]2[C:17]([CH3:18])=[C:16]([CH3:19])[NH:15][C:14]=12)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:20][CH:21]=[C:22]([Cl:25])[CH2:23]Cl>>[CH2:1]([O:8][C:9]1[N:10]=[N:11][CH:12]=[C:13]2[C:17]([CH3:18])=[C:16]([CH3:19])[N:15]([CH2:23][C:22]([Cl:25])=[CH:21][Cl:20])[C:14]=12)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Procedure

The title compound was prepared as ocherous powdery crystals in 8.0% yield in a similar procedure to that described in Example 41 by using 7-benzyloxy-2,3-dimethylpyrrolo[2,3-d]pyridazine and 1,2,3-trichloro-1-propene.

Sources & evidence

ORD record
ord-d7f0dfd88fcf48a4abe0ca993894e6d2
Source dataset
uspto-grants-2000_05
Patent number
US06063782

Linked notes

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