HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220379Generated: October 31, 2026
N-Iodosuccinimide → HCID 58180567, compound
https://huagongshe.com/reaction/220379
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 58180565 | HCID 58180565 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 58180567 | HCID 58180567 | — |
Reaction Steps
N,N-Dicyclopropyl-4-(3-(1,3-dimethyl-1H-pyrazol-5-yl)thioureido)-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (example 41B, 41 mg, 0.083 mmol) was dissolved in chloroform (2780 μL) and cooled to 0° C. NIS (18.76 mg, 0.083 mmol) was slowly added and the reaction was warmed to room temperature. The reaction mixture was concentrated. Methanol and ether were added and the mixture was filtered. After standing for a week, product precipitated out of the solution. The product was triturated with methanol. N,N-Dicyclopropyl-4-(1,3-dimethyl-1H-pyrazolo[3,4-d]thiazol-5-ylamino)-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide was isolated as a pale yellow solid (8.1 mg, 20% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202881B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-143d632151fa454caad110cc55c0c349 |
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| Source note | uspto-grants-2012_06 |
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