HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550974Generated: October 30, 2026
N,N,N',N'-Tetramethylethylenediamine → HCID 59166727, compound
https://huagongshe.com/reaction/550974
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 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 | — |
| Product | HCID 59166727 | HCID 59166727 | — |
Reaction Steps
Butyllithium (2.5 M in hexanes, 0.29 ml, 0.74 mmol) was added to a stirred solution of 4-chloro-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one from Step B (50 mg, 0.295 mmol) at −78° C. in THY (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 mg, 0.295 mmol, described in Intermediate 2) was added and the reaction warmed to ambient temperature. After 8 h, the reaction was quenched with H2O and the mixture was partitioned between EtOAc and H2O. 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 | US07947677B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-60ad9b4fe48c42bdb91d1e7a0dfcfd3b |
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| Source note | uspto-grants-2011_05 |
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