Methanol → HCID 178493814, compound
Reaction equation
[NH2:1][C:2]1[C:3]([C:15]([OH:17])=O)=[CH:4][C:5]2[O:10][CH:9](COC)[CH2:8][O:7][C:6]=2[CH:14]=1.[N:18]1[CH:23]=CC=NN=1.N1CCCCC1.[CH3:30][OH:31]>>[CH3:30][O:31][CH:9]1[O:10][C:5]2[CH:4]=[C:3]3[C:2](=[CH:14][C:6]=2[O:7][CH2:8]1)[N:1]=[CH:23][N:18]=[C:15]3[OH:17]Participants
5
Procedure
The titled compound of Example 5 (0.367 g, 1.53 mmol), triazine (0.19 g, 2.3 mmol) and piperidine (0.015 ml, 0.153 mmol) was dissolved in 10 ml of methanol, followed by refluxing for 4 hours to obtain a white solid, which was then cooled down to a room temperature. The solid compound was filtered, washed with methanol and dried under vacuum to prepare the titled compound (0.240 g, 63%, m.p. 246-251° C.).
Workup
- temperatureby refluxing for 4 hours
- customto obtain a white solid, which
- filtrationThe solid compound was filtered
- washwashed with methanol
- customdried under vacuum
- customto prepare the titled compound (0.240 g, 63%, m.p. 246-251° C.)
Sources & evidence
- ORD record
- ord-ee1db21b02d64757861454f8b7c9a72a
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06835735B2
Reaction notes
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