4-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine → 5-(3-Chloro-2-fluorophenyl)-6-(5-chloropyridin-2-yl)-2-(2-(dimethylamino)-4-methoxypyrimidin-5-yl)-1-isopropyl-5,6-dihydropyrrolo[3,4-b]pyrrol-4(1H)-one

HRID 2204419Notes

Reaction equation

HRID 2204419 reaction equation
Br[C:2]1[N:6]([CH:7]([CH3:9])[CH3:8])[C:5]2[CH:10]([C:22]3[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][N:23]=3)[N:11]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([Cl:20])[C:15]=3[F:21])[C:12](=[O:13])[C:4]=2[CH:3]=1.[CH3:29][O:30][C:31]1[C:36](B2OC(C)(C)C(C)(C)O2)=[CH:35][N:34]=[C:33]([N:46]([CH3:48])[CH3:47])[N:32]=1.BrC1N(C(C)C)C2C(C3C=CC(Cl)=CC=3)N(C3C=C(Cl)C=CC=3C)C(=O)C=2C=1.COC1C(B2OC(C)(C)C(C)(C)O2)=CN=C(N)N=1>>[Cl:20][C:16]1[C:15]([F:21])=[C:14]([N:11]2[C:12](=[O:13])[C:4]3[CH:3]=[C:2]([C:36]4[C:31]([O:30][CH3:29])=[N:32][C:33]([N:46]([CH3:47])[CH3:48])=[N:34][CH:35]=4)[N:6]([CH:7]([CH3:9])[CH3:8])[C:5]=3[CH:10]2[C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][N:23]=2)[CH:19]=[CH:18][CH:17]=1

Participants

5

Reactant 4

HCID 591984044-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amineHCID 722213904-Methoxy-N,N-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)pyrimidin-2-amine2×HCID 867031662-Bromo-5-(3-chloro-2-fluorophenyl)-6-(5-chloropyridin-2-yl)-1-isopropyl-5,6-dihydropyrrolo[3,4-b]pyrrol-4(1H)-oneHCID 867031692-bromo-5-(5-chloro-2-methyl-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one

Product 1

HCID 867032405-(3-Chloro-2-fluorophenyl)-6-(5-chloropyridin-2-yl)-2-(2-(dimethylamino)-4-methoxypyrimidin-5-yl)-1-isopropyl-5,6-dihydropyrrolo[3,4-b]pyrrol-4(1H)-one

Procedure

The title compound was prepared in analogy to the procedure described for Example 25 but 2-bromo-5-(3-chloro-2-fluorophenyl)-6-(5-chloropyridin-2-yl)-1-isopropyl-5,6-dihydropyrrolo[3,4-b]pyrrol-4(1H)-one (Intermediate BT) and 4-methoxy-N,N-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine (Intermediate W) were used instead of 2-bromo-5-(5-chloro-2-methyl-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-b]pyrrol-4-one and 4-methoxy-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrimidin-2-ylamine respectively. The title compound was obtained as a brown solid. ESI-MS: tR=1.32 min, [M+H]+ 555/557/559 (LC-MS 1).

Workup

  1. customThe title compound was prepared in analogy to the procedure

Sources & evidence

ORD record
ord-65f24e0076674d2f8d6dc84b9bd89bee
Source dataset
uspto-grants-2016_06
Patent number
US09365576B2

Reaction notes

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