HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710272Generated: October 29, 2026
Diisopropylethylamine → (S)-tert-Butyl 2-(4-(2,5-dichloropyrimidin-4-ylamino)phenyl)morpholine-4-carboxylate
https://huagongshe.com/reaction/710272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4,5-Trichloropyrimidine | HCID 237259 | — |
| Reactant | (S)-Tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylate | HCID 66705988 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (S)-tert-Butyl 2-(4-(2,5-dichloropyrimidin-4-ylamino)phenyl)morpholine-4-carboxylate | HCID 86671412 | — |
Reaction Steps
A mixture of (S)-tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylate (100 mg, 0.36 mmol), 2,4,5-trichloropyrimidine (66 mg, 0.36 mmol) and diisopropylethylamine (70 mg, 0.54 mmol) was dissolved in 2-propanol (1.5 ml) and shaken at 80° C. overnight. Most of the solvent was evaporated. Ammonium chloride solution was added and the mixture was extracted with ethyl acetate twice. The combined organic layers are dried (MgSO4) and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181230B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-1a73a0e76d3e4552ad461879e4cba360 |
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| Source note | uspto-grants-2015_11 |
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