1-Hydroxybenzotriazole → HCID 54157151, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]3[S:25][C:24]4=[N:26][C:27]([C:29]5[CH:37]=[CH:36][C:32]([C:33]([OH:35])=[O:34])=[CH:31][CH:30]=5)=[CH:28][N:23]4[N:22]=3)=[CH:17][CH:16]=2)[CH2:11][CH2:10]1.O[N:39]1[C:43]2[CH:44]=[CH:45][CH:46]=[CH:47][C:42]=2[N:41]=[N:40]1.Cl.C(N=C=NCCCN(C)C)C>ClCCl>[N:39]1([O:34][C:33](=[O:35])[C:32]2[CH:31]=[CH:30][C:29]([C:27]3[N:26]=[C:24]4[N:23]([CH:28]=3)[N:22]=[C:21]([C:18]3[CH:17]=[CH:16][C:15]([N:12]5[CH2:11][CH2:10][CH:9]([O:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][O:2][CH3:1])[CH2:14][CH2:13]5)=[CH:20][CH:19]=3)[S:25]4)=[CH:37][CH:36]=2)[C:43]2[CH:44]=[CH:45][CH:46]=[CH:47][C:42]=2[N:41]=[N:40]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 4-[2-[4-[4-(5-methoxypentyloxy)piperidin-1-yl]phenyl]imidazo[2,1-b][1,3,4]thiadiazol-6-yl]benzoic acid (1.28 g) and 1-hydroxybenzotriazole (465 mg) in dichloromethane (50 ml) was added 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (WSCD.HCl) (943 mg), and the mixture was stirred overnight at ambient temperature. The reaction mixture was evaporated in vacuo. To the resulting precipitate was added water (50 ml), and the solid was washed with water and IPE (50 ml) and dried under reduced pressure for 3 hours to give 4-[2-[4-[4-(5-methoxypentyloxy)piperidin-1-yl]phenyl]imdazo[2,1-b][1,3,4]thiadiazol-6-yl]benzoic acid benzotriazol-1-yl ester (1.26 g).
Workup
- customThe reaction mixture was evaporated in vacuo
- additionTo the resulting precipitate was added water (50 ml)
- washthe solid was washed with water and IPE (50 ml)
- customdried under reduced pressure for 3 hours
Sources & evidence
- ORD record
- ord-659e3b7303c14ebe9641c2f71f7bbe60
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06884868B1
Reaction notes
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