HCID 18382547, compound → HCID 58289809, compound

HRID 2088754Notes

Reaction equation

HRID 2088754 reaction equation
C[N:2]1[CH2:11][C:10](C)(C)[C:9]2[C:4](=CC(N)=C[CH:8]=2)[CH2:3]1.Cl[C:16]1[N:21]=[C:20]2[N:22]([CH3:36])[C:23](=[O:35])[N:24]([C:27]3[C:32]([Cl:33])=[CH:31][CH:30]=[CH:29][C:28]=3[Cl:34])[C:25](=[NH:26])[C:19]2=[CH:18][N:17]=1.ClC1N=C2NC(=O)[N:46]([C:49]3[C:54](Cl)=[CH:53][CH:52]=[CH:51][C:50]=3Cl)C(=N)C2=CN=1>>[Cl:34][C:28]1[CH:29]=[CH:30][CH:31]=[C:32]([Cl:33])[C:27]=1[N:24]1[C:25](=[NH:26])[C:19]2[C:20](=[N:21][C:16]([NH:46][C:49]3[CH:50]=[C:51]4[C:52](=[CH:53][CH:54]=3)[C:3]3([CH2:4][CH2:9][CH2:8]3)[NH:2][CH2:11][CH2:10]4)=[N:17][CH:18]=2)[N:22]([CH3:36])[C:23]1=[O:35]

Participants

4

Reactant 3

HCID 18382547HCID 18382547, compoundHCID 582897897-chloro-3-(2,6-dichlorophenyl)-4-imino-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 178507161HCID 178507161, compound

Product 1

HCID 58289809HCID 58289809, compound

Procedure

70 mg of the entitled compound was obtained as a white solid according to the same method as in Example 2, for which, however, 3′,4′-dihydro-2′H-spiro[cyclobutane-1,1′-isoquinolin]-6′-amine obtained in Production Example 30 was used in place of 2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinolin-7-amine in Example 2, and 7-chloro-3-(2,6-dichlorophenyl)-4-imino-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one obtained in Production Example 7 was used in place of 7-chloro-3-(2,6-dichlorophenyl)-4-imino-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one.

Workup

  1. customobtained in Production Example 7

Sources & evidence

ORD record
ord-0b2322809fd44c01be31486cd5110ce6
Source dataset
uspto-grants-2013_05
Patent number
US08436004B2

Reaction notes

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