HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899314Generated: October 29, 2026
N-Aminomorpholine → HCID 58747011, compound
https://huagongshe.com/reaction/899314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Aminomorpholine | HCID 20315 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 58747008 | HCID 58747008 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 58747011 | HCID 58747011 | — |
Reaction Steps
Trimethylaluminum (2M solution in toluene, 625 microliters, 1.25 mmol) is added to a solution of 4-aminomorpholine (121 microliters, 1.25 mmol) in CHCl3 (3 ml) at room temperature. The reaction mixture was stirred for 1 h, then 4-amino-1-(2-chlorophenyl)-5-(4-chlorophenyl)-1H-pyrazole-3-carboxylic acid ethyl ester (I-2A-1a, 188 mg, 0.5 mmol) was added in one portion. The reaction mixture was stirred at 45° C. for 4 h, cooled to room temperature, and quenched with 1 M HCl (1 ml) (CAREFUL: gas evolution). The pH of the solution was adjusted to ˜13 using 25% KOH, at which point all solids went into solution. The aqueous solution was extracted with EtOAc (2×) and the combined organic solution was washed with saturated aqueous brine, dried, and concentrated under vacuum to give the product I-10A-1a as an amorphous solid (208 mg): MS 432.0 (M+1)+; 1H NMR (400 MHz, CDCl3) δ 7.44-7.32 (m, 4H), 7.28-7.23 (m, 2H), 7.13-7.09 (m, 2H), 3.86 (m, 4H), 2.95 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354929B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-393612c77e534a9a84b2c6d0cbbe23e1 |
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| Source note | uspto-grants-2008_04 |
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