HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916773Generated: October 30, 2026
4-Methylmorpholine → HCID 67219505, compound
https://huagongshe.com/reaction/916773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | (3-Mercapto-phenyl)-carbamic acid tert-butyl ester | HCID 11436060 | — |
| Reactant | 7-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 67219524 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67219505 | HCID 67219505 | 85% |
Reaction Steps
To a round bottom flask with DMF (5 mL), was added 7-Cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine, CuI, N-methylmorphline and (3-Mercapto-phenyl)-carbamic acid tert-butyl ester. The reaction was heated at 110° C. overnight. After cooling to room temperature, the reaction mixture was extracted with EtOAc (80 mL) and saturated sodium bicarbonate solution (60 ml). The organic layer was washed with water, brine, dried over sodium sulfate and concentrated. Purification through flash column afforded the product as a light yellow solid (108 mg, 85%). MS: 426.1 (MH+); HPLC Rf: 6.332 min.; HPLC purity: 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07271262B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-e2fbbe01a4f74a518d381d49c9c5b314 |
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| Source note | uspto-grants-2007_09 |
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