HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170418Generated: November 2, 2026
HCID 68525551, compound → HCID 68764170, compound
https://huagongshe.com/reaction/1170418
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 68525551 | HCID 68525551 | — |
| Reactant | HCID 68767644 | HCID 68767644 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68764170 | HCID 68764170 | — |
Reaction Steps
A solution of [(R)-3-(3-Amino-4-hydroxy-phenyl)-1-(di-tert-butoxy-phosphoryloxymethyl)-1-methyl-propyl]-carbamic acid tert-butyl ester (157.5 mg, 0.313 mmol) and 3-ethoxy-benzimidic acid ethyl ester hydrochloride in dry methanol (2 mL) was stirred for 20 minutes at 120° C. in a closed vial (microwave reactor). After cooling to RT the precipitate was filtered off, washed 2× with MeOH, 3× with water and 3× with diethyl ether. After drying in vacuum, the precipitate was dissolved in a mixture of diethyl ether/HCl (4 mL, 2M) and methanol (1 mL). After evaporation of the solvents the title compound was obtained as colorless crystals. 1H-NMR (CD3OD): δ=7.76 (d; 1H), 7.71 (s; 1H), 7.61 (bs; 2H), 7.47 (m; 1H), 7.37 (m; 1H), 7.14 (d; 1H), 4.24-4.00 (m; 4H), 2.89 (m; 2H), 2.10 (m; 2H), 1.47 (s; 6H); MS (ESI+): 421.4 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825260B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-b336a2f79c2f4b41a022b12b88f63122 |
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| Source note | uspto-grants-2010_11 |
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