HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038820Generated: November 1, 2026
Trifluoroacetic acid → HCID 66980615, compound
https://huagongshe.com/reaction/1038820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 67130023 | HCID 67130023 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66980615 | HCID 66980615 | — |
Reaction Steps
A flask was charged with 1-(7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-N-(2,4-dimethoxybenzyl)methanamine (1.0 g, 2.6 mmol, prepared using H from 7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine-3-carbaldehyde [WO 03/076427, Preparation 138] with 2,4-dimethoxybenzylamine), DCM (20 mL) and TFA (10 mL). To the mixture was added triethylsilane (0.50 mL, 3.1 mmol) and the mixture was heated to about 55° C. for about 6 h. The solvents were removed under reduced pressure to give (7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)methanamine 2,2,2-trifluoroacetate (1.6 g) as a crude material that was used directly without further purification: LC/MS (Table 2, Method h) Rt=1.65 min; MS m/z: 243 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551981B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-a0158801283b4b54bf6974fc282fbcae |
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| Source note | uspto-grants-2013_10 |
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