HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169555Generated: November 2, 2026
Water → (R)-tert-butyl 2-(2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)acetate
https://huagongshe.com/reaction/2169555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | (R)-2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine | HCID 86670088 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-tert-butyl 2-(2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)acetate | HCID 86670103 | 67.2% |
Reaction Steps
Sodium hydride (60% in oil, 19.41 mg, 0.485 mmol) was added to a solution of (R)-2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine (PREPARATION x3, 100 mg, 0.441 mmol) in DMF (1 mL) at 0° C. The resulting mixture was stirred at room temperature for 30 minutes, after which tert-butyl bromoacetate (0.078 mL, 0.529 mmol) was added at 0° C. The reaction mixture was stirred at room temperature for 30 minutes. Water was added and the mixture was extracted with EtOAc, washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, 20-80% EtOAc/hexane gradient) to afford the title compound as an off-white solid (101 mg, 67.2%). 1H NMR (400 MHz, CDCl3) δ 1.44-1.49 (m, 9 H), 3.01-3.11 (m, 1 H), 3.15-3.29 (m, 2 H), 3.37 (dd, J=11.37, 8.84 Hz, 1 H), 3.58 (td, J=11.94, 2.91 Hz, 1 H), 3.64-3.76 (m, 2 H), 3.88-4.07 (m, 3 H), 4.53 (dd, J=13.89, 2.02 Hz, 1 H), 7.22 (s, 1 H). ESI-MS m/z [M+H]+ calc'd for C15H21ClN4O3, 341.13; found 341.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09045496B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-fd9da485612a4e89af0ecb4fc04d60dc |
|---|
| Source note | uspto-grants-2015_06 |
|---|