Hydrochloric Acid → HCID 18187862, compound

HRID 1862658Notes

Reaction equation

HRID 1862658 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-a618d1dd6c224529a5fd3713f85ad073
Source dataset
uspto-grants-2003_03
Patent number
US06538002B1

Reaction notes

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