Sodium Hydroxide → HCID 86683040, compound

HRID 1497217Notes

Reaction equation

C([O:3][C:4]([C:6]1[C:7]([O:25][CH:26]([CH3:31])[C:27]([F:30])([F:29])[F:28])=[N:8][C:9]2[C:14]([C:15]=1[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[Cl:23])=[CH:13][C:12]([Cl:24])=[CH:11][CH:10]=2)=[O:5])C.[OH-].[Na+]>>[Cl:24][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([O:25][CH:26]([CH3:31])[C:27]([F:28])([F:30])[F:29])[C:6]([C:4]([OH:5])=[O:3])=[C:15]2[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[Cl:23]

Participants

Reactant 2

HCID 14798Sodium Hydroxide

HCID 86683039HCID 86683039, compound

Product 1

HCID 86683040HCID 86683040, compound

Procedure

The title compound was prepared in analogy to example 12 step B from 6-chloro-4-(2-chloro-benzyl)-2-(2,2,2-trifluoro-1-methyl-ethoxy)-quinoline-3-carboxylic acid ethyl ester (35 mg, 0.074 mmol) and 1N NaOH. Pale brown solid (21 mg, 64%). LC-MS (ESI): 442 (M+H)+.

Sources & evidence

ORD record: ord-6516fde6002945ac8595cb46254675dc
Source dataset: uspto-grants-2015_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09199938B2

Reaction notes

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