HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212025Generated: November 2, 2026
(S)-(4-(3,4-Dichlorobenzyl)morpholin-2-YL)methanamine → n-{[(2s)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-[5-(4-fluorophenyl)-1,2,4oxadiazol-3-yl]acetamide
https://huagongshe.com/reaction/2212025
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-(4-(3,4-Dichlorobenzyl)morpholin-2-YL)methanamine | HCID 10171585 | — |
| Reactant | Methyl (5-(4-fluorophenyl)-1,2,4-oxadiazol-3-yl]acetate | HCID 85817174 | — |
| Catalyst | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | n-{[(2s)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-[5-(4-fluorophenyl)-1,2,4oxadiazol-3-yl]acetamide | HCID 68880198 | 57.4% |
Reaction Steps
A mixture of Intermediate 38 (0.024 g), Intermediate 9 (0.025 g), and 1-methyl-2-pyrrolidinone (1 drop) was subjected was subjected to irradiation in a 600 W microwave oven on full power for 4 mins. The reaction mixture was dissolved in methanol and applied to an ion exchange cartridge (2 g Isolute SCX, pre-conditioned with methanol). Elution with methanol (3 column volumes) followed 10% 0.880 ammonia in methanol (2 column volumes) and evaporation of the first basic fraction in vacuo gave the crude product. Purification by Biotage flash column chromatography on silica gel (8 g cartridge), eluting with 100:8:1 dichloromethane/ethanol/0.880 ammonia, gave the title compound as a white solid (0.025 g). LCMS (System A) Rf 2.85 min Mass Spectrum m/z 479, 481 [MH+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101882B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-b7237dedf4304fe6a8fdb8ecdd4c9e3c |
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| Source note | uspto-grants-2006_09 |
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