HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 6-Iodo-7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 7-Methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-one | HCID 597065 | — |
| Reactant | HCID 66753972 | HCID 66753972 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Iodo-7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one | HCID 66753571 | — |
Reaction Steps
A stirred solution of Step 1 Intermediate (20 g, 120.463 mmol) in acetonitrile (200 ml) was treated with ceric ammonium nitrate (33 g, 60.233 mmol) and iodine (18 g, 72.281 mmol) at room temperature according to the procedure outlined in Intermediate 1, Step 3 to give 35 g of the product as a light yellow solid; 1H NMR (300 MHz, DMSO-d6) δ 2.56 (s, 3H), 7.52 (d, J=5.1 Hz, 1H), 7.97 (d, J=4.8 Hz, 1H); ESI-MS (m/z) 291.29 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119647B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-ed55976fa2264f37944e536d84f6d7b5 |
| Source note | uspto-grants-2012_02 |