HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873775Generated: October 27, 2026
Diisopropylethylamine → tert-butyl N-[N-[2-(2,6-dimethylphenoxy)acetyl]carbamimidoyl]carbamate
https://huagongshe.com/reaction/873775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2,6-Dimethylphenoxy)acetic acid | HCID 101369 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | Tert-butyl amino(imino)methylcarbamate | HCID 86691067 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-butyl N-[N-[2-(2,6-dimethylphenoxy)acetyl]carbamimidoyl]carbamate | HCID 149434096 | 94% |
Reaction Steps
(2,6-Dimethylphenoxy)acetic acid (5.41 g; 30 mmol), diisopropylethylamine (19.39 g; 150 mmol), tert-butyl amino(imino)methylcarbamate (5.73 g; 36 mmol), and 1-hydroxybenzotriazole monohydrate (5.52 g; 36 mmol) were dissolved in N,N-dimethylformamide (120 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (13.66 g; 36 mmol) was added thereto, and the mixture was stirred for 65 hours at room temperature. To the reaction solution, ethyl acetate (400 mL) was added, and the mixture was washed with 10% aqueous citric acid solution, brine, saturated aqueous sodium bicarbonate solution, and then brine. The organic layer was dried over anhydrous magnesium sulfate and then distilled under reduced pressure. The resulting crystals were dispersed in diethyl ether, collected by filtration and dried to give 9.03 g of the title compound (yield 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975411B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-320524c1c0524f128ac0d46c9b25fbe3 |
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| Source note | uspto-grants-2015_03 |
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