HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375085Generated: November 2, 2026
Diisopropylethylamine → HCID 69419383, compound
https://huagongshe.com/reaction/1375085
Participants
| Role | Name | HCID | Charge |
|---|
| 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-Methoxy-4-o-tolylureidophenylacetic acid | HCID 11449840 | — |
| Reactant | [2-(4-Amino-phenyl)-indan-2-yl]-acetic Acid Ethyl Ester | HCID 69419599 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69419383 | HCID 69419383 | 19% |
Reaction Steps
A solution of [2-(4-amino-phenyl)-indan-2-yl]-acetic acid ethyl ester (0.158 g, Reference Example 10) in dimethylformamide (2 mL) was treated with a solution of [3-methoxy-4-(3-o-tolyl-ureido)-phenyl]-acetic acid (0.169 g) in dimethylformamide (2 mL) which had been treated with diisopropylethylamine (1.3 mL) and a solution of O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (0.223 g) in dimethylformamide (2 mL). After stirring at room temperature for 2 hours the reaction mixture was evaporated and the residue was partitioned between ethyl acetate (30 mL) and hydrochloric acid (30 mL, 0.5N). The organic phase was washed with hydrochloric acid (30 mL, 0.5N), then with saturated sodium hydrogen carbonate solution (30 mL), then dried over magnesium sulfate and then evaporated. The residual beige coloured solid was subjected to chromatography on silica eluting with a mixture of ethyl acetate and cyclohexane (2:1, v/v) to give the title compound (0.06 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166616B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-b0119a1b56204874adefe6de50e8ead5 |
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| Source note | uspto-grants-2007_01 |
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