HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985069Generated: November 1, 2026
Glutaric anhydride → HCID 60043797, compound
https://huagongshe.com/reaction/1985069
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 60206856 | HCID 60206856 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 60043797 | HCID 60043797 | 32% |
Reaction Steps
To a solution of 3-amino-4-(3,5-difluoro-phenyl)-1-(7-ethyl-1,2,3,4-tetrahydro-naphthalen-1-ylamino)-butan-2-ol (0.240 g, 0.64 mmol), triethylamine (0.268 mL, 1.92 mmol), and chloroform (3 mL) was added glutaric anhydride (0.073 g, 0.64 mmol) and reaction was stirred overnight at 60° C. Reaction was washed with 1N HCl, 10% NaHCO3, brine, dried over MgSO4, filtered, concentrated in vacuo to give 5-[((1S,2R)-1-(3,5-difluorobenzyl)-3-{[(1S)-7-ethyl-1,2,3,4-tetrahydronaphthalen-1-yl]amino}-2-hydroxypropyl)amino]-5-oxopentanoic acid (100 mg). Purified via prep-HPLC. 1H NMR (400 MHz, CD3OD) δ 1.26 (t, J=8 Hz, 3 H), 1.73 (m, 2 H), 1.89 (m, 1 H), 2.01 (m, 1 H), 2.17 (m, 6 H), 2.68 (d, J=8 Hz, 2 H), 2.93 (d, J=6 Hz, 1 H), 3.02 (m, 1 H), 3.30 (m, 2 H), 3.88 (m, 1 H), 4.09 (m, 1 H), 4.57 (m, 1 H), 6.79 (m, 1 H), 6.88 (m, 3 H), 6.93 (d, J=6 Hz, 1 H), 7.20 (m, 2 H), 7.31 (s, 1 H); OAMS: ES+488.9 ES−486.9
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544717B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-5b8425a33bda41d88b5315c1bc2442b5 |
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| Source note | uspto-grants-2009_06 |
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