(5-Amino-1,3,4-thiadiazol-2-yl)methanol → HCID 178486112, compound
Reaction equation
[CH3:1][NH:2][C:3]([NH:5][CH2:6][CH2:7]OCC1N=CNC=1)=[S:4].N[C:16]1[S:17][C:18]([CH2:21]O)=NN=1>>[CH3:1][NH:2][C:3]([NH:5][CH2:6][CH2:7][CH2:16][S:17][CH2:18][C:21]1[N:5]=[CH:3][NH:2][CH:1]=1)=[S:4]Participants
3
Procedure
By the method of Example 58 (i) and (ii) 4(5)-hydroxymethylimidazole was converted first to the intermediate 4(5)-[(3-aminopropyl)thiomethyl]-imidazole dihydrobromide and thence to the title compound (m.p. 118°-120° C, after recrystallisation from water).
Sources & evidence
- ORD record
- ord-2779f151de6b45d6b4500a64c77f7475
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04104382
Reaction notes
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