3,6-Dichloropyridazine → HCID 57910803, compound

HRID 1968674Notes

Reaction equation

HRID 1968674 reaction equation
[CH3:1][C:2]([C:21]1[N:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=1)([C:6]1[CH:11]=[CH:10][C:9](B2OC(C)(C)C(C)(C)O2)=[CH:8][CH:7]=1)[CH:3]([CH3:5])[CH3:4].ClC1N=NC(C2C=CC(C(C)(C3C=CC(OCC4C=CC=CN=4)=CN=3)C(C)C)=CC=2)=CC=1.Cl[C:61]1[N:62]=[N:63][C:64]([C:67]([F:70])([F:69])[F:68])=[CH:65][CH:66]=1.CC(C1C=CC(OCC2C=CC=CN=2)=CN=1)(C1C=CC(B2OC(C)(C)C(C)(C)O2)=CC=1)C(C)C.ClC1N=NC(Cl)=CC=1>>[CH3:1][C:2]([C:21]1[N:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=1)([C:6]1[CH:7]=[CH:8][C:9]([C:61]2[N:62]=[N:63][C:64]([C:67]([F:70])([F:69])[F:68])=[CH:65][CH:66]=2)=[CH:10][CH:11]=1)[CH:3]([CH3:4])[CH3:5]

Participants

6

Reactant 5

HCID 673313,6-DichloropyridazineHCID 282425263-Chloro-6-(trifluoromethyl)pyridazineHCID 579107912-{1,2-Dimethyl-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propyl}-5-(pyridin-2-ylmethoxy)pyridineHCID 579108026-{1,2-Dimethyl-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propyl}pyridin-3-olHCID 57910808HCID 57910808, compound

Product 1

HCID 57910803HCID 57910803, compound

Procedure

Compound 8b was prepared from 8a following procedures similar to those described for preparing compound 5b substituting compound 8a and 3-chloro-6-trifluoromethylpyridazine for compound 5a and 3,6-dichloropyridazine, respectively. m/z (ES) 402 (MH)+

Sources & evidence

ORD record
ord-461e143b09804c65bedd6fffb699357c
Source dataset
uspto-grants-2013_04
Patent number
US08426413B2

Reaction notes

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