Tetrahydropyran-4-ylacetic acid → HCID 11269753, compound
Reaction equation
[O:1]1[CH2:7][CH:6]([C:8]2[C:16]3[S:15][C:14]([NH2:17])=[N:13][C:12]=3[C:11]([O:18][CH3:19])=[CH:10][CH:9]=2)[CH2:5][O:4][CH2:3][CH2:2]1.[O:20]1[CH2:25][CH2:24][CH:23]([CH2:26][C:27](O)=[O:28])[CH2:22][CH2:21]1>>[O:4]1[CH2:5][CH:6]([C:8]2[C:16]3[S:15][C:14]([NH:17][C:27](=[O:28])[CH2:26][CH:23]4[CH2:24][CH2:25][O:20][CH2:21][CH2:22]4)=[N:13][C:12]=3[C:11]([O:18][CH3:19])=[CH:10][CH:9]=2)[CH2:7][O:1][CH2:2][CH2:3]1Participants
3
Procedure
Using 7-[1,4]dioxepan-6-yl-4-methoxy-benzothiazol-2-ylamine and tetrahydropyran-4-yl acetic acid, the tide compound was prepared as white powder. MS: m/e=407(M+H+).
Workup
- customthe tide compound was prepared as white powder
Sources & evidence
- ORD record
- ord-01c5b2b551c8492fa867466d61ff131b
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07371748B2
Reaction notes
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