Ethylene carbonate → 4-(2-Hydroxyethoxy)-2-amino-1,3-benzoxazol
Reaction equation
[OH:1][C:2]1[C:7]2[N:8]=[C:9]([NH2:11])[O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.C1(=O)O[CH2:15][CH2:14][O:13]1>>[OH:13][CH2:14][CH2:15][O:1][C:2]1[C:7]2[N:8]=[C:9]([NH2:11])[O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
The title compound was prepared according to the procedure of Example 91, Step 1, starting from 4-hydroxy-2-amino-1,3-benzoxazol*(0.97 g, 6.5 mmol) and ethylene carbonate (0.63 g, 7.1 mmol). Solid; yield 46%; mp 124-126° C. Anal. (C9H10N2O3) C, H, N.
Sources & evidence
- ORD record
- ord-c401697294ae4fec9e6ff7729b9cf9ee
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07071180B2
Reaction notes
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