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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111961Generated: November 3, 2026

3-Bromophenyl isocyanate → HCID 178521749, compound

https://huagongshe.com/reaction/2111961

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromophenyl isocyanateHCID 141001—
ReactantHCID 178518960HCID 178518960—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 178521749HCID 178521749157%

Reaction Steps

2-Amino-4-chloro-benzoic acid (17.16 g, 100 mmol) was suspended in 90 ml of water and 20 ml of concentrated HCl. NaNO2 (6.9 g, 100 mmol) was dissolved in 15 ml water and added slowly at 0° C. The mixture was stirred at 0° C. for 30 minutes and Na2SO3 (34.0 g, 270 mmol) were added, dissolved in 150 ml water. The mixture was then stirred for 2 hours at room temperature. 30 ml of concentrated HCl were added and the mixture stirred overnight at room temperature and then at 80° C. for 2 hours. The solution is treated with aqueous NaOH until the pH is 5.5 and the precipitated was filtered and triturated with ethanol to yield 13.8 g (82%) of 6-chloro-1H-indazol-3-ol. 6-Chloro-1H-indazol-3-ol (700 mg, 4.15 mmol) was dissolved in 25 ml pyridine together with 1-bromo-3-isocyanato-benzene (990 mg, 5 mmol) and stirred at RT for 4 hours. The mixture was then diluted with EtOAc (100 ml) and washed 2× with 1 M HCl. The organic phase was dried with Na2SO4 and reduced under vacuum. The residue was now dissolved in 1 M NaOH and washed with EtOAc and then precipitated with HCl and the precipitate extracted into EtOAc, dried and reduced under vacuum. The product was then recrystallised from EtOAc and heptane to yield 1.1 g (79%) of crystalline solid (m.p. 223-225° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521480B2
Source datasetuspto-grants-2009_04
ORD IDord-c9d2c73a40964ac2b62ed2c0ae54b017
Source noteuspto-grants-2009_04