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Hydrochloric Acid → HCID 66841583, compound

HRID 1929014
Notes
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Reaction equation

HRID 1929014 reaction equation
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][C@H:15]2[C@@H:24]3[N:19]([CH2:20][CH2:21][CH2:22][CH2:23]3)[CH2:18][CH2:17][CH2:16]2)[CH2:10][CH2:9]1)(C)(C)C.[ClH:26]>O1CCOCC1>[ClH:26].[ClH:26].[ClH:26].[C@H:15]1([CH2:14][N:11]2[CH2:12][CH2:13][CH:8]([NH2:7])[CH2:9][CH2:10]2)[C@@H:24]2[N:19]([CH2:20][CH2:21][CH2:22][CH2:23]2)[CH2:18][CH2:17][CH2:16]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric Acid2×HCID 59600141{1-[(1S,9aR)-1-(Octahydro-quinolizin-1-yl)methyl]-piperidin-4-yl}-carbamic acid tert-butyl ester

Product 1

HCID 66841583HCID 66841583, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Procedure

The ester 62 (3.8 g, 10.8 mmol) is dissolved in 15 ml of dioxane and after addition of 70 ml of a 4M solution of HCl in do of HCl in dioxan the mixture is stirred for 4 hours at RT. The product is filtered off and is used in the next step without further purification.

Workup

  1. filtrationThe product is filtered off
  2. customis used in the next step without further purification

Sources & evidence

ORD record
ord-279f2d2379b241eab17ea6e685cfc3de
Source dataset
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08183366B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes