Isopropylamine → HCID 53860405, compound
Reaction equation
[CH2:1]([O:5][C:6]([NH:8][CH:9]=[CH:10][C:11]1[CH:21]=[CH:20][C:14]([O:15][CH2:16][CH:17]2[O:19][CH2:18]2)=[CH:13][CH:12]=1)=[O:7])[CH2:2][CH2:3][CH3:4].[CH:22]([NH2:25])([CH3:24])[CH3:23]>C(O)(C)C>[CH2:1]([O:5][C:6]([NH:8][CH:9]=[CH:10][C:11]1[CH:21]=[CH:20][C:14]([O:15][CH2:16][CH:17]([OH:19])[CH2:18][NH:25][CH:22]([CH3:24])[CH3:23])=[CH:13][CH:12]=1)=[O:7])[CH2:2][CH2:3][CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Analogously to the description in Example 2, 3.93 g (0.0135 mol) of 1-[p-(2-n-butoxycarbonylaminovinyl)-phenoxy]-2,3-epoxy-propane, on reaction with 1.22 ml (0.0142 mol) of isopropylamine in 50 ml of isopropanol, yield 1-[p-(2-n-butoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-isopropylaminopropane of melting point of 125°-126° C. (from acetone-ether).
Sources & evidence
- ORD record
- ord-040c4f8b974e49bb8283d3da7c1f0398
- Source dataset
- uspto-grants-1977_07
- Patent number
- US04038414
Reaction notes
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