Hydrochloric Acid → HCID 18187862, compound

HRID 278213Notes

Reaction equation

HRID 278213 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][CH2:16][C:17]2[CH:18]=[N:19][C:20]3[C:25]([CH:26]=2)=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:27]>CO>[ClH:27].[ClH:27].[N:19]1[C:20]2[C:25](=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:26]=[C:17]([CH2:16][CH2:15][CH2:14][CH:11]2[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]2)[CH:18]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 18187735HCID 18187735, compound

Product 1

HCID 18187862HCID 18187862, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A solution of 1-(t-butoxycarbonyl)-4-(3-(quinolin-3-yl)propyl)piperidine from Step A (240 mg, 0.68 mmol) in 1M HCl solution (8 mL) in methanol was stirred at rt for 48 h. The solution was concentrated and the residue crystallized from ethyl acetate to afford the title compound (182 mg),

Workup

  1. concentrationThe solution was concentrated
  2. customthe residue crystallized from ethyl acetate

Sources & evidence

ORD record
ord-c69722b8a727498aba062bc813a1d126
Source dataset
uspto-grants-2002_03
Patent number
US06358979B1

Reaction notes

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