HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172683Generated: November 2, 2026
N,N-Dimethylethylenediamine → HCID 71230972, compound
https://huagongshe.com/reaction/2172683
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-[5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzoic acid | HCID 10491405 | — |
| Reactant | (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate | HCID 75951468 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71230972 | HCID 71230972 | 79.9% |
Reaction Steps
To a suspension of Intermediate 12b (1 g, 3.87 mmol) in DCM (20 ml) was added COMU (1.891 g, 4.26 mmol) and DIPEA (0.812 ml, 4.65 mmol). The yellow solution was stirred for 2 min at rt and turned red. 2-Dimethylaminoethylamine (0.518 ml, 4.65 mmol) was added and the reaction mixture was stirred at reflux for 1 hr. After cooling to rt, the mixture was washed with water, saturated aqueous NH4Cl and extrated with EtOAc. The organic layer was dried over Na2SO4 and the solvent was removed in vacuo. The crude product was purified by flash chromatography (ISCO CombiFlash Rf, 120 g silicagel; A=dichloromethane, B=DCM:7N NH3 in MeOH (9:1), 2% hold for 5 min, gradient to 50% B over 15 min). Fractions containing the product where combined to yield 1.355 g. The final product (1.015 g) was obtained after crystallisation from heptane as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056843B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-939cd4ccdd5a47ceae382044c987c40e |
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| Source note | uspto-grants-2015_06 |
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