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Hydrochloric Acid → HCID 178518552, compound

HRID 2406138
Notes
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Reaction equation

HRID 2406138 reaction equation
CC[O-].[Na+].O=[C:6]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH:7]1[C:14]([O:16]CC)=O.[NH2:19][C:20]([NH2:22])=[S:21].Cl>CCO>[SH:21][C:20]1[N:19]=[C:14]([OH:16])[C:7]2[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:6]=2[N:22]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 227421Ethyl 2-oxocyclooctane-1-carboxylateHCID 2723790ThioureaHCID 2723922Sodium ethoxide

Product 1

HCID 178518552HCID 178518552, compoundYield 63.2%

Reagents, catalysts & solvents 1

HCID 702Ethanol
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
Solvent

Procedure

700 mg of NaOEt (10 mmol; 1.0 equiv) was added to 6 mL of abs. EtOH. To this solution was added, with stirring, 2 g of ethyl 2-keto-cyclooctylcarboxylate (10 mmol; 1.0 equiv) and 1 g of thiourea (13 mmol; 1.3 equiv). The mixture was refluxed for 6 hours. After cooling, the mixture was poured onto ice and acidified with hydrochloric acid. 1.33 g of 2-mercapto-5,6,7,8,9,10-hexahydrocycloocta[d]-pyrimidine-4-ol (63% yield) was obtained as a white solid.

Workup

  1. additionTo this solution was added
  2. temperatureThe mixture was refluxed for 6 hours
  3. temperatureAfter cooling
  4. additionthe mixture was poured onto ice

Sources & evidence

ORD record
ord-6411807fe0c24e6ba130524acb1d3fb6
Source dataset
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08809347B2

Reaction notes

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