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Sodium hydrosulfide → HCID 178499044, compound

HRID 973831
Notes
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Reaction equation

HRID 973831 reaction equation
Cl[C:2]1[N:7]2[N:8]=[C:9]([C:11]([O:13][CH3:14])=[O:12])[N:10]=[C:6]2[N:5]=[C:4]([CH:15]([CH3:17])[CH3:16])[CH:3]=1.[SH-:18].[Na+]>O>[CH:15]([C:4]1[CH:3]=[C:2]([SH:18])[N:7]2[N:8]=[C:9]([C:11]([O:13][CH3:14])=[O:12])[N:10]=[C:6]2[N:5]=1)([CH3:17])[CH3:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 28015Sodium hydrosulfideHCID 16767691Methyl 7-chloro-5-(propan-2-yl)-(1,2,4)triazolo(1,5-a)pyrimidine-2-carboxylate

Product 1

HCID 178499044HCID 178499044, compoundYield 90.8%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The product obtained in Step 2 (40 g) was added at 0° C. to a solution of sodium hydrosulfide (40 g) in one liter of water with stirring under a nitrogen stream. The mixture was stirred at 0° C. for one hour, then at room temperature for three hours, and the resulting yellow solution was washed with 200 ml of ethyl acetate. The aqueous layer was acidified with concentrated hydrochloric acid to pH 2.0, and the formed crystals were collected by filtration and washed with 100 ml of ethanol, affording 36 g of the objective compound as faint yellow crystals.

Workup

  1. stirringThe mixture was stirred at 0° C. for one hour
  2. washthe resulting yellow solution was washed with 200 ml of ethyl acetate
  3. filtrationthe formed crystals were collected by filtration
  4. washwashed with 100 ml of ethanol

Sources & evidence

ORD record
ord-d865621457e049aca3126a068a0cb194
Source dataset
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05064953

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes