2-Furanmethanethiol → HCID 23462916, compound
Reaction equation
[CH2:1]([SH:7])[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.Br.[CH3:9][N:10]1[CH2:16][CH2:15][C:14]2=[CH:17][C:18](=[O:22])[C:19](=[O:21])[CH:20]=[C:13]2[CH2:12][CH2:11]1>CO>[OH:22][C:18]1[C:19]([OH:21])=[CH:20][C:13]2[CH2:12][CH2:11][N:10]([CH3:9])[CH2:16][CH2:15][C:14]=2[C:17]=1[S:7][CH2:1][C:2]1[O:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the procedures outlined in Example 17, 0.9 g. (0.0075 mole) of furfuryl mercaptan and 2 g. (0.0073 mole) of 3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-dione hydrobromide were reacted in 200 ml. of methanol to yield 7,8-dihydroxy-6-furfurylthio-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine, free base m.p. 162°-165° C.
Sources & evidence
- ORD record
- ord-4c06edc0efd344a197c42d6c6f141056
- Source dataset
- uspto-grants-1981_05
- Patent number
- US04265890
Reaction notes
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