HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162919Generated: October 29, 2026
1,2-Benzenediamine, N1-ethyl- → HCID 11856842, compound
https://huagongshe.com/reaction/1162919
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Benzenediamine, N1-ethyl- | HCID 90275 | — |
| Reactant | HCID 57557962 | HCID 57557962 | — |
| Product | HCID 11856842 | HCID 11856842 | 74.2% |
Reaction Steps
Purified water (0.01 ml) and TFA (0.01 ml) were added to a dichloromethane solution that contained the 7-((R)-5-hydroxymethyl-2-oxooxazolidin-3-yl)-3-diethoxymethyl-2H-isoquinolin-1-one (3.3 mg, 0.009 mmol) prepared in step C. The obtained mixture was left at a room temperature for 30 minutes, and the reaction solution was concentrated. The obtained yellow solid and an ethanol solution that contained N-ethyl-1,2-benzenediamine (1.2 mg, 0.009 mmol), which was a known compound described in a publication (Leicester Polytech; Synthetic Communications, vol. 19(7-8), p. 1381, (1989)), were heated to reflux for 17 hours. Thereafter, the reaction solution was concentrated. The obtained residue was purified by preparative silica gel TLC (dichloromethane:methanol=20:1), so as to obtain 3-(1-ethyl-1H-benzoimidazol-2-yl)-7-((R)-5-hydroxymethyl-2-oxooxazolidin-3-yl)-2H-isoquinolin-1-one (2.7 mg, yield: 74%) in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820693B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-5062ef1ab4db41f6b8e4bf80f79a0273 |
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| Source note | uspto-grants-2010_10 |
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