HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268801Generated: October 30, 2026
4-Methylmorpholine → HCID 178501380, compound
https://huagongshe.com/reaction/2268801
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | HCID 69806827 | HCID 69806827 | — |
| Reactant | HCID 178524460 | HCID 178524460 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178501380 | HCID 178501380 | 93% |
Reaction Steps
A solution of O-(2,6dichlorobenzyl)-L-tyrosine methyl ester hydrochloride (2.50 g, 6.4 mmol), 2-mercaptonicotinic acid (0.99 g, 6.4 mmol) and NMM (1.41 ml, 1.29 g, 12.8 mmol) in DMF (10 ml) was stirred at room temperature for 64 h. Solvent was removed in vacuo and the residue partitioned between DCM (30 ml) and water (25 ml). The aqueous layer was extracted with DCM (30 ml) and the combined organic layers were washed with 10% NaHCO3 solution (30 ml), dried over MgSO4 and the solvent removed in vacuo to give a brown oil which was purified by chromatography (SiO2; gradient elution, 4:1 EtOAc/hexane to 100% EtOAc) to give the title compound as a yellow foam, (2.92 g, 93%). δH (CDCl3) 8.71 (1H, dd, J 1.8, 7.6Hz), 8.05 (1H, s), 7.61 (1H, dd, J 1.8, 6.1 Hz), 7.35 (2H, m), 7.33-7.19 (2H, m), 6.94 (2H, d, J 8.7Hz), 5.22 (2H, s), 4.97 (1H, m), 3.74 (3H, s) and 3.21 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329372B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-9eb107e6a3854fcdb45b2041f0372392 |
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| Source note | uspto-grants-2001_12 |
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