HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58303Generated: October 26, 2026
Diisopropylethylamine → HCID 178431866, compound
https://huagongshe.com/reaction/58303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-6-bromopurine | HCID 6101139 | — |
| Reactant | (S)-7-(1-Aminoethyl)-6-(3-fluorophenyl)-3-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one | HCID 58111427 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178431866 | HCID 178431866 | 19% |
Reaction Steps
A solution of 7-[(1S)-1-aminoethyl]-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.10 g, 0.33 mmol) and 2-amino-6-bromopurine (0.11 g, 0.49 mmol) in 1-butanol (0.66 mL) was treated with N,N-diisopropylethylamine (86 μL, 0.49 mmol), degassed with nitrogen for 5 min and heated at 100° C. for 18 hours. The reaction was not complete and was, therefore, heated at 115° C. for an additional 5 hours. The reaction mixture was diluted with methanol (10 mL), stirred, and filtered. The filtrate was purified by RP-HPLC (XBridge C18 column, eluting with a gradient of acetonitrile/water containing 0.1% ammonium hydroxide, at flow rate of 60 mL/min) to give the desired product (27 mg, 19%) as a white solid. LCMS for C20H18FN8OS (M+H)+: m/z=437.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434746B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-fcb69ff54468406c9d81b23d6312234e |
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| Source note | uspto-grants-2016_09 |
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