2-Furoyl isothiocyanate → HCID 22397380, compound
Reaction equation
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([N:8]=[C:9]=[S:10])=[O:7].[NH2:11][CH2:12][CH2:13][CH2:14][CH2:15][N:16]1[C:24]2[CH:23]=[C:22]([CH3:25])[N:21]=[C:20]([NH2:26])[C:19]=2[N:18]=[C:17]1[CH2:27][O:28][CH2:29][CH3:30]>>[NH2:26][C:20]1[C:19]2[N:18]=[C:17]([CH2:27][O:28][CH2:29][CH3:30])[N:16]([CH2:15][CH2:14][CH2:13][CH2:12][NH:11][C:9]([NH:8][C:6]([C:2]3[O:1][CH:5]=[CH:4][CH:3]=3)=[O:7])=[S:10])[C:24]=2[CH:23]=[C:22]([CH3:25])[N:21]=1Participants
3
Procedure
Using the method of Examples 36-45, 2-furoylisothiocyanate was reacted with 1-(4-aminobutyl)-2-ethoxymethyl-6-methyl-1H-imidazo[4,5-c]pyridin-4-amine to provide the desired compound. The observed accurate mass was 431.887.
Sources & evidence
- ORD record
- ord-6bf7d2a87443435d9d962ea1c8232a57
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06720334B2
Reaction notes
Loading…