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Guanidine Hydrochloride → HCID 14718745, compound

HRID 1088308
Notes
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Reaction equation

HRID 1088308 reaction equation
C[O-].[Na+].Cl.[NH2:5][C:6]([NH2:8])=[NH:7].CN(C)[CH:11]=[C:12]([CH:22]=O)[CH:13]([CH:19]([CH3:21])[CH3:20])[C:14]([O:16][CH2:17][CH3:18])=[O:15]>C(O)C>[NH2:7][C:6]1[N:8]=[CH:11][C:12]([CH:13]([CH:19]([CH3:20])[CH3:21])[C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:22][N:5]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 5742Guanidine HydrochlorideHCID 10942334Sodium MethoxideHCID 54210763ethyl (RS)-4-dimethylamino-3-formyl-2-(1-methylethyl)-3-butenoate

Product 1

HCID 14718745HCID 14718745, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

A solution of sodium methoxide (0.9 g) in ethanol (5 cm3) was added dropwise to a stirred suspension of guanidine hydrochloride (1.58 g) and ethyl (RS)-4-dimethylamino-3-formyl-2-(1-methylethyl)-3-butenoate in ethanol (10 cm3). The reaction mixture was heated at the reflux temperature for 2 hours, then stood at the ambient temperature for 70 hours. The solvent was evaporated under reduced pressure and water added to the residue.

Workup

  1. temperatureThe reaction mixture was heated at the reflux temperature for 2 hours
  2. customThe solvent was evaporated under reduced pressure and water
  3. additionadded to the residue

Sources & evidence

ORD record
ord-4a21f77aebe246cf90072f3b2426c1d1
Source dataset
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04962109

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes