HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036845Generated: October 30, 2026
Diisopropylethylamine → HCID 67055921, compound
https://huagongshe.com/reaction/2036845
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 2,2,5-trimethyl-1,3-dioxane-5-carboxylic Acid | HCID 11355776 | — |
| Reactant | 3-Aminobiphenyl-2-carboxamide | HCID 66965572 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67055921 | HCID 67055921 | 28.9% |
Reaction Steps
To a solution of the commercially available 2,2,5-trimethyl-1,3-dioxane-5-carboxylic acid (0.6 g, 4 mmol) in DCM (30 mL) was added HATU (1.8 g, 4.7 mmol) and DIPEA (1.6 mL, 23.5 mmol). The reaction mixture was stirred at room temperature for 1 h. After this time, 3-aminobiphenyl-2-carboxamide (0.6 g, 2.35 mmol) was added and the resulting solution was stirred for 16 h. At the conclusion of this period, the reaction mixture was washed with water, dried, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (25% ethyl acetate in hexanes) to yield N-(2-carbamoylbiphenyl-3-yl)-2,2,5-trimethyl-1,3-dioxane-5-carboxamide (0.25 g, 24% yield) as a white solid. LCMS Method Y: retention time 1.69 min; [M+1]=367.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575184B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-6ac0517f75c446a7b0a09517b67fe7ac |
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| Source note | uspto-grants-2013_11 |
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