HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (5-Chloro-7-morpholinothiazolo[4,5-d]pyrimidin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Chloro-7-morpholinothiazolo[4,5-d]pyrimidine-2-carbaldehyde | HCID 57685392 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-Chloro-7-morpholinothiazolo[4,5-d]pyrimidin-2-yl)methanol | HCID 57685397 | — |
Reaction Steps
A solution of 5-chloro-7-morpholinothiazolo[4,5-d]pyrimidine-2-carbaldehyde 43 (1.0 g, 3.5 mmol) in MeOH (30 mL) at 0° C. was treated with NaBH4 (0.1 g, 3.5 mmol). The solution was allowed to warm to room temperature and stirred 15 min. The reaction mixture was quenched with a mixture of a saturated solution of sodium bicarbonate and water (1:1, v/v). The aqueous solution was extracted with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The crude (5-chloro-7-morpholinothiazolo[4,5-d]pyrimidin-2-yl)methanol 56 required no further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893059B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-fbacf4ce09bf43ea934eb2a94d0b9048 |
| Source note | uspto-grants-2011_02 |