HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308604Generated: October 31, 2026
Ethyl bromoacetate → HCID 70424500, compound
https://huagongshe.com/reaction/2308604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | HCID 10611049 | HCID 10611049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70424500 | HCID 70424500 | 72% |
Reaction Steps
A solution of 1.3 ml of ethyl bromoacetate in 30 ml of dimethylformamide was added to a warmed solution of 6 g of 8β-aminomethyl-6-methyl-ergoline in 90 ml of dimethylformamide. At the end of the reaction, the solution was reduced in volume by evaporation in vacuo, poured into iced water and extracted with chloroform. The organic layer was removed in vacuo and the residue was purified by column chromatography on silica gel, using ethyl acetate:methanol (9:1 by volume) as eluent, to give 3.5 g of 6-methyl-8β-(N-ethoxycarbonylmethyl-aminomethyl)-ergoline (II: R1 =R2 =R3 =H, R4 =CH3, n=1, A=CHR6, R6 =H, B=CO2C2H5), m.p. 174°-176° C., after crystallization from diethyl ether. 3.5 of 6-methyl-8β-(N-ethoxycarbonylmethyl-aminomethyl)-ergoline were treated with 1.75 g of potassium cyanate, as described in Example 1, and the title compound, m.p. >300° C., was obtained in 72% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04690929 |
|---|
| Source dataset | uspto-grants-1987_09 |
|---|
| ORD ID | ord-29c9b51d3a5f4507989a04d6236eadcc |
|---|
| Source note | uspto-grants-1987_09 |
|---|