1-Hydroxybenzotriazole → HCID 54157151, compound

HRID 1816699Notes

Reaction equation

HRID 1816699 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]1

Participants

5

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

  1. customThe reaction mixture was evaporated in vacuo
  2. additionTo the resulting precipitate was added water (50 ml)
  3. washthe solid was washed with water and IPE (50 ml)
  4. 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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