HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669679Generated: October 30, 2026
1,2-Bis(bromomethyl)-4-nitrobenzene → HCID 59166727, compound
https://huagongshe.com/reaction/1669679
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Bis(bromomethyl)-4-nitrobenzene | HCID 10852360 | — |
| Reactant | 4-chloro-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one | HCID 12095870 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59166727 | HCID 59166727 | — |
Reaction Steps
Butyllithium (0.29 ml, 0.74 mmol, 2.5 M) was added to a stirred solution of 4-chloro-5,7-dihydro-6H-pyrrolo [2,3-d]pyrimidin-6-one from Step B (50.0 mg, 0.295 mmol) at −78° C. in THF (30 mL). After complete addition of butyllithium, N,N,N′N′-tetramethylethane-1,2-diamine (0.31 mL, 0.77 mmol) was added. After 1 h at −78° C., 1,2-bis(bromomethyl)-4-nitrobenzene (91.0 mg, 0.295 mmol, described in Intermediate 4) was added and the reaction warmed to ambient temperature. After 8 h, the reaction was quenched with H2O (2 mL) and the mixture was partitioned between EtOAc (50 mL) and H2O (50 mL). The aqueous solution was extracted with EtOAc (3×20 mL). The combined organic extracts were washed with brine (100 mL), dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS: m/z=317 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989624B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-467225a996324475919257f6bdadf403 |
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| Source note | uspto-grants-2011_08 |
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