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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195089Generated: October 31, 2026

Cyanamide → HCID 15239022, compound

https://huagongshe.com/reaction/1195089

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 numberUS05110347
Source datasetuspto-grants-1992_05
ORD IDord-91a6ac34b42148ed8d01a5bf172e7763
Source noteuspto-grants-1992_05