HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256191Generated: October 25, 2026
3-Bromoaniline → N-(3-bromophenyl)-7H-purin-6-amine
https://huagongshe.com/reaction/2256191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | 6-Chloropurine | HCID 5359277 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-(3-bromophenyl)-7H-purin-6-amine | HCID 9814520 | 102.8% |
Reaction Steps
A mixture of 6-chloropurine (1.0 g, 6.47 mmol), 3-bromoaniline (0.78 mL, 7.12 mmol), and conc HCl (4 drops) in isopropanol (10 mL) is stirred at 80° C. for 5 h. Upon cooling, it precipitates. The solid is filtered and washed with isopropanol and air dried to yield N6 -(3-bromophenyl)adenine (1.93 g, 91%) as a light yellow solid. 1H NMR (DMSO) δ 11.38 (1H, s), 8.78 (1H, s), 8.75 (1H, s), 7.90 (1H, d, J=8.0 Hz), 7.38-7.34 (2H, m). ##STR15##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654307 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-13fb9e9504744c84bc4e335f6c995865 |
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| Source note | uspto-grants-1997_08 |
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