HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793749Generated: October 31, 2026
HCID 58666633, compound → HCID 22021459, compound
https://huagongshe.com/reaction/1793749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58666633 | HCID 58666633 | — |
| Reactant | HCID 135681558 | HCID 135681558 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22021459 | HCID 22021459 | 35% |
Reaction Steps
4-Hydroxy-3-(1-tert-butyloxycarbonyl-4-methyl-6-morpholin-4-yl-1H-benzoimidazol-2-yl)-1,5-dihydro-pyrrol-2-one (0.032 g, 0.059 mmol) was reacted as described in the procedure used to synthesize (S)-4-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-3-(1-tert-butyloxycarbonyl-4-methyl-6-morpholin-4-yl-1H-benzoimidazol-2-yl)-1-trifluoromethanesulfonyl-1,5-dihydro-pyrrol-2-one and by using acetonitrile instead of N,N-dimethylformamide. This gave the title material (0.018 g, 35%). LCMS (+ESI, M+H+) m/z 730; 1H NMR (400 MHz, methanol-d4) δ (ppm): 1.55 (9H, s), 2.57 (3H, s), 3.20 (4H, m), 3.40 (2H, d, J=5.9 Hz), 3.85 (7H, m), 4.31 (1H, d, J=17.5 Hz), 4.44 (1H, d, J=17.6 Hz), 4.72 (1H, t, J=5.7 Hz), 7.02–7.04 (2H, m), 7.18 (1H, s), 7.30 (1H, d, J=8.4 Hz), 7.44 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081454B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-726b6a0725b1421a8ba3f63c4b0f73c4 |
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| Source note | uspto-grants-2006_07 |
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