HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755021Generated: October 28, 2026
Diisopropylethylamine → HCID 66816696, compound
https://huagongshe.com/reaction/1755021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | HCID 66817739 | HCID 66817739 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66816696 | HCID 66816696 | 61% |
Reaction Steps
N,N-Diisopropylethylamine (31.4 μL, 0.185 mmol) and 2-chloro-1-methylpyridinium iodide (18.9 mg, 0.074 mmol) were added to a solution of (3-methyl-4-{(E)-2-[2-(4-methyl-cyclohexyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-sulfonyl]-vinyl}-phenyl)-acetic acid (30.0 mg, 0.062 mmol) in dichloromethane (0.5 mL) and DMF (0.1 mL), and the mixture was stirred for 10 minutes. A 2.0 M ammonia-methanol solution (0.15 mL, 0.308 mmol) and DMAP (0.8 mg, 0.006 mmol) were then added, and the mixture was stirred overnight. The reaction mixture was then quenched by adding a saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was sequentially washed with water and saturated brine, and then dried over anhydrous Na2SO4 and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 2-(3-methyl-4-{(E)-2-[2-(4-methyl-cyclohexyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-sulfonyl]-vinyl}-phenyl)-acetamide as a white powder (18.3 mg, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169254B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-2b4922818f2349db8186f95277d9747d |
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| Source note | uspto-grants-2015_10 |
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