HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182212Generated: November 2, 2026
2-Morpholinoethylamine → HCID 86588190, compound
https://huagongshe.com/reaction/1182212
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | HCID 1499213 | HCID 1499213 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 86588190 | HCID 86588190 | 60% |
Reaction Steps
To a solution of N-aminoethylmorpholine (228 mg, 10 mmole) in 2 mL anhydrous THF at −40° C. was added 0.8 mL of 2 M n-BuLi solution in cyclohexane. Some white solid was precipitated instantly. The suspension was stirred for about a half an hour. When the bath temperature reached −10° C., a solution of 5-phenylamino-[1,2,3]thiadiazole-4-carboxylic acid ethyl ester (60 mg, 0.24 mmole) in anhydrous THF was added to the mixture. After it was stirred at room temperature for an hour, the reaction was quenched with saturated NH4Cl solution. The solution was extracted with EtOAc and residue obtained after the removal of EtOAc was purified by preparative TLC (silica gel, CH2Cl2:MeOH=15:1). The title compound was isolated as a white powder in 60% yield (48 mg). 1H NMR (ppm, in CDCl3): 10.91 (br. s, 1H), 7.77 (br. s, 1H), 7.00-7.60 (m, 5H), 3.70 (m, 4H), 2.60 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288556B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-0612473642a34ec799a3e9c0e45b053b |
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| Source note | uspto-grants-2007_10 |
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