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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274210Generated: November 1, 2026

Cyanamide → HCID 15239022, compound

https://huagongshe.com/reaction/274210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
Reactant2-Bromo-4-methyl-6-nitroanilineHCID 2775306—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
ProductHCID 15239022HCID 1523902251.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 13.0 g (56.3 mmol) of 2-bromo-4-methyl-6-nitroaniline stirring in a mixture of 25 ml glacial acetic acid and 5 ml of concentrated hydrochloric acid at 80° C., 29.0 g (690.5 mmol) of cyanamide and 25 ml of concentrated hydrochloric acid were added simultaneously, separately, and very slowly. At one point during the addition, a vigorous exotherm occurred and the external heat immediately removed. After the addition, the reaction was heated at reflux for 15 minutes. On cooling to about 50° C., 100 ml of 25% aqueous sodium hydroxide were added dropwise and the mixture heated at reflux 15 minutes. The reaction was cooled to room temperature, the insoluble orange solid filtered and washed with water followed by ethyl acetate to afford 7.4 g of yellow 3-amino-5-bromo-7-methyl-1,2,4-benzotriazine-1-oxide after drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389600
Source datasetuspto-grants-1995_02
ORD IDord-c0c43d1f5a4140f0907303c196d1ba75
Source noteuspto-grants-1995_02