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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396910Generated: October 29, 2026

Cyanamide → HCID 508624, compound

https://huagongshe.com/reaction/396910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 3006320HCID 3006320—
SolventMethanolHCID 887—
ProductHCID 508624HCID 50862465%

Reaction Steps

To a stirred solution of thioamide Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-Nα-[N′α-(4-methylbenzenesulfonyl)-L-thiotryptophanyl]-L-lysine (240 mg, 0.33 mmol, example 73) in MeOH (3 mL) was added cyanamide (28 mg, 0.66 mmol). The mixture was stirred for 5 min, then mercuric acetate (209 mg, 0.66 mmol) was added. The reaction was stirred for 3 h then diluted with saturated NH4Cl and extracted with EtOAc. The organic layer was washed with brine and concentrated then rediluted with THF/MeOH (2 mL/1 mL) and treated with 1N NaOH (0.8 mL). After stirring for 4 h, the reaction was acidified with 1N HCl and extracted with EtOAc. The organic layer was dried over MgSO4, concentrated and purified by column chromatography to give 154 mg (65%) of the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608100B1
Source datasetuspto-grants-2003_08
ORD IDord-1feb8c067cba464e90ef21655be24e04
Source noteuspto-grants-2003_08