HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930668Generated: October 31, 2026
Acetic Acid → N4-Ethyl-6-methyl-N2-(4-(oxazol-5-yl)phenyl)-N4-((tetrahydrofuran-2-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diamine
https://huagongshe.com/reaction/1930668
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N4-Ethyl-N2-(4-(oxazol-5-yl)phenyl)-N4-((tetrahydrofuran-2-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diamine | HCID 59333759 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N4-Ethyl-6-methyl-N2-(4-(oxazol-5-yl)phenyl)-N4-((tetrahydrofuran-2-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diamine | HCID 46199742 | — |
Reaction Steps
N4-Ethyl-N2-(4-(oxazol-5-yl)phenyl)-N4-((tetrahydrofuran-2-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diamine (125 mg, 0.30 mmol, example 81a) was dissolved in methanol (3 mL). Acetic acid (0.017 mL, 0.30 mmol) was added followed by formaldehyde (0.022 mL, 0.30 mmol). The reaction was stirred at room temperature for 15 minutes and sodium cyanoborohydride (18.7 mg, 0.30 mmol) (MP—CNBH3) was added. The reaction was stirred overnight at room temperature. The MP—CNBH3 was filtered, the solvent evaporated under reduced pressure, the crude dissolved in methanol and purified by preparative HPLC N4-ethyl-6-methyl-N2-(4-(oxazol-5-yl)phenyl)-N4-((tetrahydrofuran-2-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diamine (29.8 mg, 21.04%) as acetate salt. MS (ES+) m/z 435.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188101B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-ec60bacc885f434e9023e78971b9cfbf |
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| Source note | uspto-grants-2012_05 |
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