HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628113Generated: October 29, 2026
Chloroacetaldehyde → HCID 58382132, compound
https://huagongshe.com/reaction/1628113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | HCID 58382020 | HCID 58382020 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58382132 | HCID 58382132 | 52.2% |
Reaction Steps
1-(4-(2-Amino-7-ethyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-6-yl)phenyl)ethanone (0.217 g, 0.529 mmol) in EtOH (5 mL) was treated with 2-chloroacetaldehyde (˜50 wt % solution in water, 0.100 g, 0.634 mmol). The mixture was heated to about 80° C. for about 2 h then cooled to rt and concentrated under reduced pressure. The material was purified by on a 10 gram silica column with EtOAc then 9:1 DCM/MeOH as eluents to give 1-(4-(1-ethyl-3-((2-(trimethylsilyl)ethoxy)methyl)-3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-2-yl)phenyl)ethanone (0.12 g, 52%): LC/MS (Table 2, Method a) Rt=3.06 min; MS m/z 435 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785639B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-4c94404edc314dcd932c6ea13b57b80f |
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| Source note | uspto-grants-2014_07 |
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