5-Amino-3-chloro-1-methyl-1,2-dihydropyridin-2-one → ethyl 4-((5-chloro-1-methyl-6-oxo-1,6-dihydropyridin-3-ylamino)(4-chlorophenyl)methyl)-1-cyclopropyl-5-methyl-1H-pyrazole-3-carboxylate

HRID 873817Notes

Reaction equation

HRID 873817 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8](O)[C:9]2[C:10]([C:18]([O:20][CH2:21][CH3:22])=[O:19])=[N:11][N:12]([CH:15]3[CH2:17][CH2:16]3)[C:13]=2[CH3:14])=[CH:4][CH:3]=1.[NH2:24][C:25]1[CH:26]=[C:27]([Cl:33])[C:28](=[O:32])[N:29]([CH3:31])[CH:30]=1>C(Cl)Cl.CO>[Cl:33][C:27]1[C:28](=[O:32])[N:29]([CH3:31])[CH:30]=[C:25]([NH:24][CH:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)[C:9]2[C:10]([C:18]([O:20][CH2:21][CH3:22])=[O:19])=[N:11][N:12]([CH:15]3[CH2:17][CH2:16]3)[C:13]=2[CH3:14])[CH:26]=1

Participants

4

Procedure

The title compound was prepared in analogy to the procedure described in Step 10.3 using ethyl 4-((4-chlorophenyl)(hydroxy)methyl)-1-cyclopropyl-5-methyl-1H-pyrazole-3-carboxylate (Step 17.5) and 5-amino-3-chloro-1-methylpyridin-2(1H)-one (Step 5.2). tR: 4.81 min (HPLC 1); tR: 1.09 min (LC-MS 2); ESI-MS: 475/477 [M+H]+ (LC-MS 2); Rf=0.52 (CH2Cl2/MeOH 9:1).

Sources & evidence

ORD record
ord-715238e9b0654175b351172a3d656318
Source dataset
uspto-grants-2015_03
Patent number
US08975417B2

Reaction notes

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