HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945636Generated: October 31, 2026
Sodium triacetoxyborohydride → HCID 59605752, compound
https://huagongshe.com/reaction/1945636
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-(oxan-4-yl)azetidine hydrochloride | HCID 17785643 | — |
| Reactant | 2-Chloro-9-methyl-6-morpholino-9H-purine-8-carbaldehyde | HCID 59603472 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 59605752 | HCID 59605752 | 45% |
Reaction Steps
A 25 mL round-bottomed flask was charged with a solution of 2-chloro-9-methyl-6-morpholin-4-yl-9H-purine-8-carbaldehyde (0.173 g, 0.65 mmol), 3-(tetrahydropyran-4-yl)azetidine hydrochloride (0.138 g, 0.78 mmol) and 4 Å molecular sieves (0.9 g) in DCE (7 mL). The reaction mixture was stirred for 5 h at room temperature. Sodium triacetoxyborohydride (0.274 g, 1.29 mmol) was added and the reaction mixture was stirred for 18 h at room temperature. The suspension was filtered through Celite and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography (Si—PPC, MeOH:EtOAc, gradient 0:100 to 10:90) to give 2-Chloro-9-methyl-6-morpholin-4-yl-8-[3-(tetrahydropyran-4-yl)azetidin-1-ylmethyl]-9H-purine as a white foam (0.117 g, 45%). LCMS (Method A): RT=2.40 min, [M+H]+ 407.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394796B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-5d2187bb4f314c25876345bbd77453ae |
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| Source note | uspto-grants-2013_03 |
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