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HCID 10594703, compound → HCID 15391002, compound

HRID 1935403
Notes
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Reaction equation

HRID 1935403 reaction equation
C(OC([N:8]1[C@@H:13]([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:12][N:11]([C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:19]=2[CH3:25])[C:10](=[O:26])[CH2:9]1)=O)(C)(C)C>C(OCC)(=O)C>[CH2:14]([C@H:13]1[CH2:12][N:11]([C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:19]=2[CH3:25])[C:10](=[O:26])[CH2:9][NH:8]1)[CH2:15][CH2:16][CH3:17]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 10594703HCID 10594703, compound

Product 1

HCID 15391002HCID 15391002, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
0 °C

Procedure

A solution of the product from Step D (0.570 g, 1.58 mmol) in ethyl acetate (50 mL) was cooled to −15° C. under nitrogen. HCl gas was bubbled through for 15 min, and the reaction solution warmed to 0° C. for 2h. The solvent was removed in vacuo to provide the titled product.

Workup

  1. customwas bubbled through for 15 min
  • customThe solvent was removed in vacuo
  • Sources & evidence

    ORD record
    ord-a99e841a89df45269a172638b37d1ac1
    Source dataset
    uspto-grants-2002_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06387903B1

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes