HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368958Generated: November 4, 2026
Bromotrichloromethane → HCID 18517860, compound
https://huagongshe.com/reaction/1368958
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromotrichloromethane | HCID 6383 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 18517881 | HCID 18517881 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18517860 | HCID 18517860 | 32.8% |
Reaction Steps
A solution comprised of methyl 2-[2-(2-benzyloxycarbonylamino-4-methylvalerylamino)-1-hydroxy-4-phenylbutyl]-4,5-dihydrooxazole-4-carboxylate (0.036 g, 0.067 mmol) in methylene chloride (3 mL) was cooled to 0° C. and then DBU (11.2 mg, 72.7 μmol) and bromotrichloromethane (14.6 mg, 73.7 μmol) were added. The mixture was stirred for 6 hours at room temperature and concentrated. The residue was dissolved in ethyl acetate (20 mL) and the solution was dried (MgSO4) and concentrated. The product was purified from the residue by flash chromatography eluting with 1:3 hexanes/ethyl acetate to provide methyl 2-[2-(2-benzyloxycarbonylamino-4-methylvalerylamino)-1-hydroxy-4-phenylbutyl]oxazole-4-carboxylate (12 mg, 0.022 mmol) as a white solid. MS(PCI) m/z=538 (M+1) 1H NMR (CDCl3): δ 0.8-1.05 (d, J=4 Hz, 6H), δ 1.55-1.70 (m, 3H), δ 2.00 (m, 1H), δ 2.40 (m, 1H), δ 2.69 (m, 2H), δ 3.99 (m, 3H) 4.45 (m, 1H), δ 5.17 (s, 2H), δ 5.78 (m, 1H, δ 7.01 (d, J=4 Hz 1H), δ 7.14-7.47 (m, 10H) 7.72(d, J=4 Hz, 1H), δ 8.40 (s, 1H). (C29H35N3O7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576630B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-a58b96e0e8b146818042d0c78318e764 |
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| Source note | uspto-grants-2003_06 |
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