Sec-Butylamine → HCID 178449218, compound
Reaction equation
[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:3][CH:2]1[CH2:11][N:12]1[CH2:17][CH2:16][CH:15]([CH2:18][N:19]([C:24]#[N:25])[C:20](=[NH:23])SC)[CH2:14][CH2:13]1.[CH:26]([NH2:30])([CH2:28][CH3:29])[CH3:27]>N1C=CC=CC=1>[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:3][CH:2]1[CH2:11][N:12]1[CH2:17][CH2:16][CH:15]([CH2:18][N:19]([C:24]#[N:25])[C:20]([NH:30][CH:26]([CH3:27])[CH2:28][CH3:29])=[NH:23])[CH2:14][CH2:13]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3 g 1-[(2,3-dihydro[4H]1,4-benzodioxin-2-yl)methyl]4-[(N-cyano S-methyl isothioureido)methyl]piperidine, 10 ml pyridine and 30 g sec butylamine are heated to the reflux. After evaporation to dryness the resulting oily product is taken up in isopropyl ethyl allowing the recovery of a solid as colourless crystalls. They are recrystallized from isopropanol.
Workup
- temperatureare heated to the reflux
- customAfter evaporation to dryness the resulting oily product
- customThey are recrystallized from isopropanol
Sources & evidence
- ORD record
- ord-a0e010d376bf43908669586e573f9cf7
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04579845
Reaction notes
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