Sodium Hydroxide → HCID 59536422, compound

HRID 445356Notes

Reaction equation

HRID 445356 reaction equation
[F:1][C:2]([F:34])([F:33])[C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:12][CH2:11][N:10]2[C:19]([NH:21][C:22]2[CH:32]=[CH:31][C:25]([C:26]([O:28]CC)=[O:27])=[CH:24][CH:23]=2)=[O:20])=[CH:5][CH:4]=1.[OH-].[Na+]>CCO>[F:33][C:2]([F:1])([F:34])[C:3]1[CH:4]=[CH:5][C:6]([C@@H:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:12][CH2:11][N:10]2[C:19]([NH:21][C:22]2[CH:32]=[CH:31][C:25]([C:26]([OH:28])=[O:27])=[CH:24][CH:23]=2)=[O:20])=[CH:7][CH:8]=1

Participants

4

Procedure

A mixture of (R)-ethyl 4-(1-(4-(trifluoromethyl)-phenyl)-1,2,3,4-tetrahydroisoquinoline-2-carboxamido)benzoate (0.210 g, 0.4 mmol) and NaOH (0.4 mL, 2 mmol) in EtOH (5 mL) was stirred at RT in 24 h. The mixture was concentrated, taken up in H2O and neutralized with 10% HCl. The white solid was collected by filtration and dried. MS (ESI, positive ion) m/z: 441 (M+1).

Workup

  1. concentrationThe mixture was concentrated
  2. filtrationThe white solid was collected by filtration
  3. customdried

Sources & evidence

ORD record
ord-e9d6471317c54e8fa1ff5d564dece624
Source dataset
uspto-grants-2013_07
Patent number
US08476297B2

Reaction notes

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