Hydrochloric Acid → 4-[7-(1-Quinolin-6-ylcyclopropyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoic acid

HRID 1257876Notes

Reaction equation

HRID 1257876 reaction equation
O.[OH-].[Li+].[N:4]1[C:13]2[C:8](=[CH:9][C:10]([C:14]3([C:17]4[N:21]5[N:22]=[C:23]([C:26]6[CH:35]=[CH:34][C:29]([C:30]([O:32]C)=[O:31])=[CH:28][CH:27]=6)[CH:24]=[N:25][C:20]5=[N:19][CH:18]=4)[CH2:16][CH2:15]3)=[CH:11][CH:12]=2)[CH:7]=[CH:6][CH:5]=1.O.Cl>C1COCC1.CO>[N:4]1[C:13]2[C:8](=[CH:9][C:10]([C:14]3([C:17]4[N:21]5[N:22]=[C:23]([C:26]6[CH:35]=[CH:34][C:29]([C:30]([OH:32])=[O:31])=[CH:28][CH:27]=6)[CH:24]=[N:25][C:20]5=[N:19][CH:18]=4)[CH2:15][CH2:16]3)=[CH:11][CH:12]=2)[CH:7]=[CH:6][CH:5]=1

Participants

7

Procedure

Lithium hydroxide monohydrate (14 mg, 0.34 mmol) was added to a solution of methyl 4-[7-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoate (30.0 mg, 0.07 mmol) in THF (0.3 mL), methanol (0.3 mL), and water (0.2 mL). The mixture was stirred at RT for 2 h and adjusted to pH 2 with conc. HCl. The volatiles were removed under reduced pressure and the residue was dried to provide the crude product which was directly used in the next step without further purification. LCMS: (M+H)=408.1.

Workup

  1. customThe volatiles were removed under reduced pressure
  2. customthe residue was dried

Sources & evidence

ORD record
ord-fa7b6af6227e4f5c9278a716b4804b51
Source dataset
uspto-grants-2013_06
Patent number
US08461330B2

Reaction notes

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