1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 18507658, compound

HRID 1356178Notes

Reaction equation

HRID 1356178 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([S:8]([CH3:10])=O)[C:5]([C:11]#[N:12])=[C:4]([C:13]2[O:14][C:15]([CH2:18][O:19][CH3:20])=[CH:16][CH:17]=2)[N:3]=1.SC[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=1.C1CCN2C(=NCCC2)CC1>COCCOC>[NH2:1][C:2]1[N:3]=[C:4]([C:13]2[O:14][C:15]([CH2:18][O:19][CH3:20])=[CH:16][CH:17]=2)[C:5]([C:11]#[N:12])=[C:6]([S:8][CH2:10][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)[N:7]=1

Participants

5

Reactant 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 1509632-PyridineethanethiolHCID 18507258HCID 18507258, compound

Product 1

HCID 18507658HCID 18507658, compound

Reagents, catalysts & solvents 1

HCID 80711,2-DimethoxyethaneSolvent

Procedure

From 2-amino-4-methanesulfinyl-6-(5-methoxymethyl-furan-2-yl)-pyrimidine-5-carbonitrile, 2-mercaptoethylpyridine and DBU in DME. ES-MS m/e (%): 368 (M+H+, 100).

Sources & evidence

ORD record
ord-d7dc729e530a4ad0a41de9f3e6a41c2f
Source dataset
uspto-grants-2003_07
Patent number
US06586441B2

Reaction notes

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