Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86705485 | HCID 86705485 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68295199 | HCID 68295199 | 95% |
Reaction Steps
To a solution of 136 (39.5 g, 128 mmol), DCM (100 mL) and MeOH (100 mL) was added 4N solution of HCl in dioxane (160 mL, 640 mmol) and stirred for 18 h. The reaction was concentrated to afford a red oil. The residue was taken up in DCM/7N methanolic NH3 (100 mL, 9:1) and the mixture was sonicated for 5 min. The inorganic salt precipitate was removed by filtration and washed with the same solvent. The filtrate was concentrated to afford a viscous red oil. The crude product was purified by SiO2 chromatography (Biotage 40 M) eluting with DCM/7N methanolic NH3 (7:1). The recovered light brown oil crystallized to form 21.2 g (95%) (S)-2-(5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-ylamino)propan-1-ol (138) as a brown solid: MS m/z (APCI-pos) M+1=209.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133187B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-cdec32f79de745579ef31de93c132ef1 |
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| Source note | uspto-grants-2015_09 |
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