HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432253Generated: October 30, 2026
Ethyl bromoacetate → HCID 22347222, compound
https://huagongshe.com/reaction/432253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178508725 | HCID 178508725 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22347222 | HCID 22347222 | 79.4% |
Reaction Steps
Sodium hydride (60%, 0.138 g, 3.45 mmol) was added to a suspension of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.750 g, 2.87 mmol) in N,N-dimethylformamide (9 mL), and the mixture was stirred at ambient temperature for 1 hour until a homogeneous solution was obtained. Ethyl bromoacetate (0.447 mL, 4.03 mmol) was added, and the mixture was stirred at ambient temperature under an atmosphere of nitrogen for 14 hours. The solvent was removed under reduced pressure and the resulting solid was triturated sequentially with water (25 mL) and then ether/petroleum ether (4:1, 50 mL) to yield ethyl 2-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate (0.791 g, 2.28 mmol) as a brown solid: 1H NMR (DMSO-d6, 400 MHz) δ 8.21 (s, 1H), 5.17 (s, 2H), 4.15 (qt, 2H), 1.20 (t, 3H); RP-HPLC (25 to 100% CH3CN in 0.1 M aqueous ammonium acetate over 10 min at 1 mL/min using a Hypersil HS C18, 250×4.6 mm column) Rt 6.87 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06660744B1 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-b87939ee5bda4d0b9bb9deb7edae8d6d |
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| Source note | uspto-grants-2003_12 |
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