HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035220Generated: October 31, 2026
Methanol → (3-(3-Methyl-4-((methylamino)methyl)phenoxy)azetidin-1-yl)(5-phenyl-1,3,4-oxadiazol-2-yl)methanone
https://huagongshe.com/reaction/1035220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Methyl-4-(1-(5-phenyl-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yloxy)benzaldehyde | HCID 58043105 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-(3-Methyl-4-((methylamino)methyl)phenoxy)azetidin-1-yl)(5-phenyl-1,3,4-oxadiazol-2-yl)methanone | HCID 56598403 | 44% |
Reaction Steps
Titanium(IV) isopropoxide (0.20 mL, 0.68 mmol) was added to a methanol solution of methylamine (0.75 mL 2M, 1.50 mmol). The resulting solution was added to 53C (162 mg, 0.45 mmol) and then methanol (1 mL) was added. After 60 min, DCM (5 mL) was added and the solution was stirred for 2 h. Sodium borohydride (21 mg, 0.56 mmol) was added and the mixture was stirred for 60 min. Water was added and the mixture was filtered through Celite and the solid was washed extensively with DCM. The filtrate was further filtered through a phase separator and the organic solution was evaporated. The product was purified by preparative HPLC (Kromasil, C8) eluting with a gradient of acetonitrile and a mixture of acetic acid and water (0.2%). The pure fractions were combined and freeze-dried twice. There was obtained 74 mg (44%) of 53 as a solid. 1NMR (500 MHz, CDCl3): δ 2.27 (s, 3H), 2.3-2.6 (m, 4H), 3.62 (m, 2H), 4.24 (dd, 1H), 4.56 (dd, 1H), 4.66 (dd, 1H), 4.99 (m, 1H), 5.04 (m, 1H), 6.49 (d, 1H), 6.54 (s, 1H), 7.15 (d, 1H), 7.46 (t, 2H), 7.51 (t, 1H), 8.08 (d, 2H), MS (APCI+) m/z 379 [M+H]+, LC purity: 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546375B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-63ad3e5d5a524e15889dfaa9e78fb1a2 |
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| Source note | uspto-grants-2013_10 |
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