Hydrochloric Acid → HCID 22097638, compound

HRID 1648273Notes

Reaction equation

HRID 1648273 reaction equation
Cl.[CH2:2]([O:4][C:5]([C:7]1[C:8]([CH2:33][N:34]2[CH:38]=[N:37][CH:36]=[N:35]2)=[N:9][C:10]2[C:15]([C:16]=1[C:17]1[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[C:19]([O:25][CH:26]([CH3:28])[CH3:27])[CH:18]=1)=[CH:14][C:13]([O:29][CH3:30])=[C:12]([O:31][CH3:32])[CH:11]=2)=[O:6])[CH3:3].[Cl:39]CCl>C(O)C>[ClH:39].[CH2:2]([O:4][C:5]([C:7]1[C:8]([CH2:33][N:34]2[CH:38]=[N:37][CH:36]=[N:35]2)=[N:9][C:10]2[C:15]([C:16]=1[C:17]1[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[C:19]([O:25][CH:26]([CH3:28])[CH3:27])[CH:18]=1)=[CH:14][C:13]([O:29][CH3:30])=[C:12]([O:31][CH3:32])[CH:11]=2)=[O:6])[CH3:3]

Participants

5

Procedure

A solution of HCl in ethanol (23%, 0.172g) was added dropwise to a suspension of 6,7-dimethoxy-4-(3-isopropoxy-4-methoxyphenyl)-2-(1,2,4-triazol-1-ylmethyl) quinoline-3-carboxylic acid ethyl ester (0.5 g) in ethanol (10ml)-dichloromethane (2 ml) at room temperature. The mixture was stirred at the same temperature for 15 minutes and concentrated under reduced pressure. The residue was treated with isopropyl ether to yield solid, which was recrystallized from ethanol to yield 6,7-dimethoxy-4-(3-isopropoxy-4-methoxyphenyl)-2-(1,2,4-triazol-1-ylmethyl) quinoline-3-carboxylic acid ethyl ester hydrochloride (0.211g, 39%) as yellow crystals having melting point of 93 to 95° C.

Workup

  1. concentrationconcentrated under reduced pressure
  2. additionThe residue was treated with isopropyl ether
  3. customto yield solid, which
  4. customwas recrystallized from ethanol

Sources & evidence

ORD record
ord-738a12c1e3994c998d2ce32a590b8095
Source dataset
uspto-grants-1995_07
Patent number
US05436247

Reaction notes

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