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Carbonic acid-guanidine (1:1) → HCID 178490297, compound

HRID 1617237
Notes
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Reaction equation

HRID 1617237 reaction equation
C(=O)(O)O.[NH2:5][C:6]([NH2:8])=[NH:7].[C:9]([CH2:11][C:12]1[CH:13]=[CH:14][C:15]([O:27][CH3:28])=[C:16]([CH:26]=1)[CH2:17][CH:18]([C:23](=O)[CH3:24])[C:19](OC)=[O:20])#[N:10]>CO>[NH2:7][C:6]1[N:8]=[C:19]([OH:20])[C:18]([CH2:17][C:16]2[CH:26]=[C:12]([CH2:11][C:9]#[N:10])[CH:13]=[CH:14][C:15]=2[O:27][CH3:28])=[C:23]([CH3:24])[N:5]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 286947Carbonic acid-guanidine (1:1)HCID 68414744Methyl 2-(5-(cyanomethyl)-2-methoxybenzyl)-3-oxobutanoate

Product 1

HCID 178490297HCID 178490297, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
50 °C

Procedure

Guanidine carbonate (5 g) was added to a stirred solution of the product from step (i) (5.01 g) in MeOH (80 mL). The suspension was heated at 50° C. for 15 h and then the solvent evaporated under reduced pressure. The residue was diluted with water (20 mL) and diethyl ether (20 mL). The resulting precipitate was collected by filtration and the solid was dried under vacuum to give the subtitle compound as an orange solid, 2.8 g.

Workup

  1. customthe solvent evaporated under reduced pressure
  2. additionThe residue was diluted with water (20 mL) and diethyl ether (20 mL)
  3. filtrationThe resulting precipitate was collected by filtration
  4. customthe solid was dried under vacuum

Sources & evidence

ORD record
ord-32c38bcd76274c9b99b71ccdb81bd37f
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08765939B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes