1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 18507354, compound

HRID 1356037Notes

Reaction equation

HRID 1356037 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[C:5]([C:13]#[N:14])=[C:4](S(C)=O)[N:3]=1.Cl.Cl.[CH3:20][C:21]1[C:22]([CH2:27][NH2:28])=[N:23][CH:24]=[CH:25][CH:26]=1.C1CCN2C(=NCCC2)CC1>COCCOC>[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[C:5]([C:13]#[N:14])=[C:4]([NH:28][CH2:27][C:22]2[C:21]([CH3:20])=[CH:26][CH:25]=[CH:24][N:23]=2)[N:3]=1

Participants

5

Reactant 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 185074241-(3-Methylpyridin-2-yl)methanamine--hydrogen chloride (1/2)HCID 185076922-Amino-4-(furan-2-YL)-6-(methylsulfinyl)pyrimidine-5-carbonitrile

Product 1

HCID 18507354HCID 18507354, compound

Reagents, catalysts & solvents 1

HCID 80711,2-DimethoxyethaneSolvent

Procedure

From 2-amino-4-furan-2-yl-6-methanesulfinyl-pyrimidine-5-carbonitrile, C-(3-methyl-pyridin-2-yl)-methylamine dihydrochloride and DBU in DME. ES-MS m/e (%): 307 (M+H+, 100).

Sources & evidence

ORD record
ord-eebb348060444c688397f8d80b53e6fc
Source dataset
uspto-grants-2003_07
Patent number
US06586441B2

Reaction notes

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