Benzoic acid, 2-hydrazinyl-, hydrochloride (1:1) → 8-Chloro-10H-benzo[4,5]furo[3,2-b]indole-1-carboxylic acid

HRID 1936829Notes

Reaction equation

HRID 1936829 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH2:8][C:7](=O)[C:6]=2[CH:11]=1.[ClH:12].[NH:13]([C:15]1[CH:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17]([OH:19])=[O:18])N>C(O)C.O>[Cl:12][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]3[C:23]4[C:15](=[C:16]([C:17]([OH:19])=[O:18])[CH:20]=[CH:21][CH:22]=4)[NH:13][C:7]=3[C:6]=2[CH:11]=1

Participants

5

Reactant 2

HCID 104169Benzoic acid, 2-hydrazinyl-, hydrochloride (1:1)HCID 105127485-Bromobenzo[b]furan-3(2H)-one

Product 1

HCID 99258878-Chloro-10H-benzo[4,5]furo[3,2-b]indole-1-carboxylic acidYield 66%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Procedure

To a solution of 5-chloro-3(2H)-benzofuranone (0.357 g, 2.12 mmol) [Ellingboe, J. et al. J. Med. Chem. 1992, 35 (7), 1176-1183] in ethanol (100 mL) was added a solution of 2-hydrazinobenzoic acid hydrochloride (0.800 g, 4.24 mmol) in deionized water (50 mL). The mixture was stirred for one hour at room temperature and then allowed to sit while cooled (0° C.). Vacuum filtration and drying in vacuo afforded 0.400 g (62%) of the title compound as a pale yellow solid: mp 190° C. (dec) which was used without further purification.

Workup

  1. temperaturewhile cooled (0° C.)
  2. filtrationVacuum filtration
  3. customdrying in vacuo

Sources & evidence

ORD record
ord-cd94d2f41b0740f3b0f70c60384788de
Source dataset
uspto-grants-2002_05
Patent number
US06391902B1

Reaction notes

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