HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059593Generated: October 30, 2026
1-Phenethylamine, (-)- → HCID 44595569, compound
https://huagongshe.com/reaction/2059593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-9-cyclopentyl-5,7,7-trimethyl-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-one | HCID 59295116 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 44595569 | HCID 44595569 | 26.3% |
Reaction Steps
2-Chloro-9-cyclopentyl-5,7,7-trimethyl-8,9-dihydro-5H-pyrimido[5,4-b][1,4]diazepin-6(7H)-one (100 mg, 0.3238 mmol, prepared as described in WO 2007/095188) was dissolved in n-butyl alcohol (1 mL). To the butyl alcohol solution thus obtained were then added (1S)-1-phenylethanamine (750 μL, 5.830 mmol) and DIPEA (167.4 mg, 225.6 μL, 1.295 mmol). The resulting solution was heated at 140° C. in microwave for 90 minutes. Additional (1S)-1-phenylethanamine (500 μL, 3.887 mmol) was added and the reaction mixture heated for 90 minutes in microwave at 140° C. The solvent was removed in vacuo and the residue dissolved in dichloromethane and washed sequentially with 0.5M HCl (three times, 5 mL each), saturated aqueous sodium hydrogen carbonate solution (three times, 5 mL each), and brine (once, 5 mL). The washed solution was dried over MgSO4, filtered, and concentrated in vacuo to give yellow oil. The oil was purified by mass directed HPLC and the product fractions passed through a bicarbonate cartridge and lypholized to afford the title compound as a white solid (33.5 mg, 26% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278297B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-fc5764578cb9446b8cf1394fa53ba43f |
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| Source note | uspto-grants-2012_10 |
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