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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225195Generated: November 1, 2026

Ammonia → HCID 15586936, compound

https://huagongshe.com/reaction/225195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
Reactant4-MethylmorpholineHCID 7972—
ReactantHCID 86737358HCID 86737358—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductHCID 15586936HCID 1558693672.4%

Reaction Steps

0.6 g (0.0021 moles) of 6-methyl-8β-hydrazino-methyl-ergoline are introduced, under vigorous stirring, into a solution of 0.28 ml (0.0025 moles) of N-methyl-morpholine in 60 ml of dry chloroform. When the solid dissolves completely, a solution of 0.184 g (0.0023 moles) of acetyl chloride in 2 ml of acetonitrile is added dropwise, within 5 minutes, to the mixture. After the addition the pH of the mixture is checked, and when it is lower than 6, N-methyl-morpholine is introduced. The reaction mixture is stirred at room temperature for one hour, thereafter it is diluted with 30 ml of water, and the pH of the mixture is adjusted to 8 with aqueous ammonia. The mixture is shaken, the phases are separated from each other, the organic phase is washed twice with water, dried, and evaporated to dryness in vacuo. The dry residue is crystallized from ethanol. The separated crystals are filtered off, washed with a small amount of cold (5° C.) ethanol, and dried in vacuo. 0.5 g (72.4%) of 6-methyl-8β-([N'-acetyl-hydrazino]-methyl)-ergoline are obtained; m.p.: 213°-215° C., [α]D20 =-38.7° (c=1, in 96% ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235912
Source datasetuspto-grants-1980_11
ORD IDord-0f174f0e889646c2b5ac0499bcbcc0a3
Source noteuspto-grants-1980_11