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Water → HCID 12939990, compound

HRID 917805
Notes
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Reaction equation

HRID 917805 reaction equation
[CH3:1][N:2]([CH3:6])[C:3](Cl)=[O:4].[Cl:7][C:8]1[CH:9]=[CH:10][C:11]2[S:15]C(NC)=[N:13][C:12]=2[CH:18]=1.[H-].[Na+].O.[CH3:22][N:23](C)[CH:24]=O>>[Cl:7][C:8]1[CH:9]=[CH:10][C:11]2[S:15][C:1]([N:2]([CH3:6])[C:3](=[O:4])[N:23]([CH3:24])[CH3:22])=[N:13][C:12]=2[CH:18]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 962WaterHCID 6228DimethylformamideHCID 6598Dimethylcarbamoyl ChlorideHCID 24758Sodium hydrideHCID 27268585-chloro-N-methyl-1,3-benzothiazol-2-amine

Product 1

HCID 12939990HCID 12939990, compound

Procedure

N,N-dimethylcarbamoylchloride (1.1g) and 5-chloro-2-methylaminobenzothiazole (2g) were dissolved in dimethylformamide (25ml) and the mixture was stirred while adding slowly sodiumhydride (0.44g, 55% oily) in a stream of nitrogen for an hour and maintaining the temperature below -5°C. After stirring 3 additional hours at the room temperature, the mixture was poured into water (100ml) and the precipitate was filtrated, washed and dried.

Workup

  1. temperaturemaintaining the temperature below -5°C
  2. stirringAfter stirring 3 additional hours at the room temperature
  3. filtrationthe precipitate was filtrated
  4. washwashed
  5. customdried

Sources & evidence

ORD record
ord-93aeb2eedfd243db89beedaef9d512b2
Source dataset
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03967950

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes