HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652609Generated: November 1, 2026
Dimethylformamide → HCID 13914704, compound
https://huagongshe.com/reaction/652609
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 13558464 | HCID 13558464 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13914704 | HCID 13914704 | — |
Reaction Steps
A mixture of 14.5 g (32.3 mmol) of 5-chloro-2-[2-[(2-hydroxyethyl)]amino]-7-(phenylmethoxy)anthra[1,9-cd]pyrazol-6(2H)-one (5) and its 10-phenylmethoxy isomer (4), ~4:1 respectively by HPLC, 3.9 ml of α-bromotoluene, 6.5 g of potassium bicarbonate, and 140 ml of N,N-dimethylformamide was stirred at room temperature for 18 hr. The mixture was diluted with 500 ml of water and extracted with three 200 ml portions of dichloromethane. The combined organic extracts were washed with water, dried, and concentrated to an oil which was purified by chromatography on 600 g of silica gel (230-400 mesh). Elution with ethyl acetate:hexane (3:2) followed by concentration of product fractions gave the faster eluting component as a solid. Crystallization from acetonitrile afforded 3.55 g of pure isomer 9, mp 130°-134° C. Elution with ethyl acetate followed by concentration of product fractions afforded 9.2 g (66%) of slower eluting isomer 8 as a syrup which could not be crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04672129 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-c2f3002fd9084668806fd50878421f63 |
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| Source note | uspto-grants-1987_06 |
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