HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390815Generated: October 27, 2026
Iodine → 2-Chloro-6-iodo-4-morpholinofuro[3,2-d]pyrimidine
https://huagongshe.com/reaction/390815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Chloro-4-morpholinofuro[3,2-d]pyrimidine | HCID 56833741 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-6-iodo-4-morpholinofuro[3,2-d]pyrimidine | HCID 59593070 | 83% |
Reaction Steps
To a solution of 2-chloro-4-morpholinofuro[3,2-d]pyrimidine 38 (50 mg, 1.0 eq) dissolved in THF (2.1 ml) at −78° C. was added 1.6M solution of n-butyllithium (0.17 ml, 1.3 eq, 1.6M in hexanes). Reaction mixture was stirred at −78° C. for 30 minutes. A solution of iodine (159 mg, 3.0 eq) in THF (0.6 ml) was added and reaction mixture was allowed to slowly warm up to room temperature and stirred for 45 minutes. The reaction mixture was quenched with saturated aq. Na2S2O3, and extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The crude reaction mixture was purified by flash chromatography to yield 2-chloro-6-iodo-4-morpholinofuro[3,2-d]pyrimidine 45 (63 mg, 83%): MS (Q1) 366 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08383620B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-5299dac637004dddb28ea8a72459849e |
|---|
| Source note | uspto-grants-2013_02 |
|---|