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Ammonia → HCID 178510518, compound

HRID 1632662
Notes
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Reaction equation

HRID 1632662 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10](=[CH:17][N:18](C)C)[C:9]2=[O:21])[CH:5]=[CH:6][CH:7]=1.N>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10](=[CH:17][NH2:18])[C:9]2=[O:21])[CH:5]=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 222AmmoniaHCID 537196081-(3-Chlorophenyl)-3-(dimethylaminomethylene)-2(1H,3H)-indolone

Product 1

HCID 178510518HCID 178510518, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Title product of Example A3 (0.3 g, 1 mmole) was stirred with 10 ml of ethanol for 3 minutes and the mixture then perfused with NH3 for 1 hour at 25°, stirred an additional 16 hours, and concentrated to an oil, which crystallized on standing in vacuo. Trituration with pentane gave purified title product, 0.25 g, m.p. 141°-143°.

Workup

  1. concentrationconcentrated to an oil, which
  2. customcrystallized
  3. customTrituration with pentane gave
  4. custompurified title product, 0.25 g, m.p. 141°-143°

Sources & evidence

ORD record
ord-3df1f2f2226f4197ac868572d8e0119d
Source dataset
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04476307

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes