Hydrazine hydrate (1:1) → 9-Bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid hydrazide

HRID 1949916Notes

Reaction equation

HRID 1949916 reaction equation
C([O:3][C:4]([C:6]1[S:7][C:8]2[CH2:9][CH2:10][O:11][C:12]3[CH:19]=[CH:18][C:17]([Br:20])=[CH:16][C:13]=3[C:14]=2[N:15]=1)=O)C.O.[NH2:22][NH2:23]>C(O)C>[Br:20][C:17]1[CH:18]=[CH:19][C:12]2[O:11][CH2:10][CH2:9][C:8]3[S:7][C:6]([C:4]([NH:22][NH2:23])=[O:3])=[N:15][C:14]=3[C:13]=2[CH:16]=1

Participants

4

Reactant 2

HCID 24654Hydrazine hydrate (1:1)HCID 67050521Ethyl 9-bromo-4,5-dihydrobenzo[2,3]oxepino[4,5-D]thiazole-2-carboxylate

Product 1

HCID 670967839-Bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid hydrazide

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Alternatively, to a suspension of 9-bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid ethyl ester (4.55 g) in ethanol (50 mL) was added hydrazine monohydrate (5 mL) and the reaction heated at reflux for 16 h. After cooling to room temperature, the solid was filtered, washed with diethyl ether and air-dried to give 9-bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid hydrazide.

Workup

  1. temperaturethe reaction heated
  2. temperatureat reflux for 16 h
  3. filtrationthe solid was filtered
  4. washwashed with diethyl ether
  5. customair-dried

Sources & evidence

ORD record
ord-69a85d795c6c4bc1a96080823f0ddbc8
Source dataset
uspto-grants-2013_03
Patent number
US08399690B2

Reaction notes

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