Triethylamine → 2-(2,6-Dimethoxypyridin-4-yl)-4-(2,4,6-trifluorobenzyl)-2H-pyrido[2,3-e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide

HRID 1772969Notes

Reaction equation

HRID 1772969 reaction equation
[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[C:6]([F:11])[C:3]=1[CH2:4][NH2:5].[C:12](N1C=CN=C1)(N1C=CN=C1)=[O:13].C([N:26](CC)CC)C.FC1C=C(OC)C=C(F)C=1CN1[C:40]2[N:41]=[CH:42][CH:43]=[CH:44][C:39]=2[S:38](=[O:46])(=[O:45])[N:37]([C:47]2[CH:52]=[CH:51]C(OC)=[C:49]([O:55][CH3:56])[CH:48]=2)[C:36]1=[O:57]>CN(C=O)C>[CH3:56][O:55][C:49]1[CH:48]=[C:47]([N:37]2[C:36](=[O:57])[N:5]([CH2:4][C:3]3[C:2]([F:1])=[CH:9][C:8]([F:10])=[CH:7][C:6]=3[F:11])[C:40]3[N:41]=[CH:42][CH:43]=[CH:44][C:39]=3[S:38]2(=[O:45])=[O:46])[CH:52]=[C:51]([O:13][CH3:12])[N:26]=1

Participants

6

Procedure

The title compound (82 mg, 0.17 mmol) was prepared in two steps from (IntC2) (165 mg, 0.5 mmol), 2,4,6-trifluorobenzylamine (0.18 mL, 1.5 mmol); followed by 1,1′-carbonyldiimidazole (233 mg, 1.44 mmol), triethylamine (0.10 mL, 0.72 mmol) in DMF (1.5 mL) using the methods of (95).

Sources & evidence

ORD record
ord-1d701fbb9c4147b0a5163813045efbde
Source dataset
uspto-grants-2016_02
Patent number
US09249160B2

Reaction notes

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