HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365824Generated: November 1, 2026
Iodine → 4-(5-Chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholine
https://huagongshe.com/reaction/1365824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 5-Chloro-7-(morpholin-4-yl)[1,3]thiazolo[4,5-d]pyrimidine | HCID 57685414 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-Chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholine | HCID 25252763 | — |
Reaction Steps
4-(5-Chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine 16 was dissolved in tetrahydrofuran and iodine (3 eq) was added. The solution was cooled to −50° C. and potassium bis(trimethylsilyl)amide (1.2 eq of 0.5M solution in toluene) was added over a period of 10 minutes. The solution was warmed to room temperature and stirred overnight. Water was added to quench the reaction and the tetrahydrofuran was removed in vacuo. The residue was brought up in methylene chloride, washed with saturated sodium bicarbonate solution and dried with magnesium sulfate. The solution was concentrated a purified by silica gel chromatography to yield 4-(5-chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholine 27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893059B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-44f349ba2ee243c3b02d4f72664edf09 |
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| Source note | uspto-grants-2011_02 |
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