HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49723Generated: October 31, 2026
Diisopropylethylamine → HCID 17946656, compound
https://huagongshe.com/reaction/49723
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 | (3-Acetoxy-4-nitro-phenyl)acetic acid | HCID 17946639 | — |
| Reactant | ethyl (3RS)-3-(5-aminopyrid-2-yl)butyrate | HCID 17946645 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 17946656 | HCID 17946656 | — |
Reaction Steps
A solution of O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (10.95 g) in dry dimethylformamide (20 mL) was added to a solution of (RS) ethyl 3-(5-aminopyrid-2-yl)butanoate (3.0 g, Reference Example 5), diisopropylethylamine (10 mL) and (3-acetoxy-4-nitro-phenyl)acetic acid (6.89 g, Reference Example 17) in dimethylformamide (90 mL) under a nitrogen atmosphere. After stirring at 30° C. for 24 hours the reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 5% aqueous sodium bicarbonate. The organic phase was washed with water, then with brine, then dried over magnesium sulphate, then treated with decolourising charcoal followed by filtration and evaporation of the filtrate to give the title compound as a dark oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706738B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-9ba64a1116f449bb9ec1ca7dc4da51be |
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| Source note | uspto-grants-2004_03 |
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