HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243303Generated: October 29, 2026
2-Bromoacetamide → HCID 178461910, compound
https://huagongshe.com/reaction/243303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178461909 | HCID 178461909 | — |
| Product | HCID 178461910 | HCID 178461910 | — |
Reaction Steps
A mixture of [(S)-1-((R)-1-piperidin-3-yl-1H-benzoimidazol-2-yl)ethyl]-(9H-purin-6-yl)amine from Example 16 (150 mg, 0.414 mmol), 2-bromo-acetamide (57 mg, 0.414 mmol) and DIPEA (215 mL, 1.24 mmol) in IMS (2 mL) was stirred in a sealed vial at 70° C. for 20 h. After cooling to RT, volatiles were removed under reduced pressure and the resulting residue was purified by column chromatography (Si—PCC, gradient 0-15% 2M NH3/MeOH in DCM). The product containing fractions were concentrated in vacuo and the resulting residue was triturated with MeOH affording 133 (59 mg, 34%). LCMS: RT 1.80 min [M+H]+ 420.1. 1H NMR (DMSO, 400 MHz): δ 8.25 (1H, s), 8.14 (1H, s), 8.01-7.90 (1H, m), 7.74-7.66 (1H, m), 7.63-7.55 (1H, m), 7.28-7.03 (4H, m), 5.95 (1H, bs), 4.75 (1H, br), 3.04-2.86 (4H, m), 2.74 (1H, bd, J=11.16 Hz), 2.24 (1H, bt, J=11.70 Hz), 1.80-1.55 (5H, m), 1.35-1.19 (1H, m)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-20f6a72351704b899bcd29f8f9ddbc1c |
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| Source note | uspto-grants-2014_02 |
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