HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879367Generated: October 28, 2026
Lithium iodide → (S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(8-oxo-1,7-naphthyridin-7(8H)-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetic acid
https://huagongshe.com/reaction/879367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(8-oxo-1,7-naphthyridin-7(8H)-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetate | HCID 86700172 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(8-oxo-1,7-naphthyridin-7(8H)-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetic acid | HCID 86700173 | — |
Reaction Steps
To a solution of (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(8-oxo-1,7-naphthyridin-7(8H)-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetate (7.9 mg, 0.012 mmol) in pyridine (0.6 mL) was added LiI (75 mg, excess). The reaction mixture was heating in a microwave at 170° C. for 90 min. The mixture was concentrated in vacuo and then purified by reverse phase HPLC, eluting by 0-100% acetonitrile in H2O with 0.1% TFA to give the desired product. LCMS-ESI+ (m/z): [M+H]+ calcd for C33H28ClN4O4S: 611.2; found: 611.2. 1H NMR (400 MHz, CDCl3) δ 9.06 (d, J=2.8 Hz, 1H), 8.68 (d, J=5.2 Hz, 1H), 8.62 (s, 1H), 8.08 (d, J=8.0 Hz, 1H), 7.99-7.92 (m, 3H), 7.76-7.69 (m, 2H), 7.55-7.49 (m, 3H), 6.66 (d, J=7.6 Hz, 1H), 5.34 (s, 1H), 2.58 (s, 3H), 1.01 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a09802ac394846de8a6d6aea433b5251 |
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| Source note | uspto-grants-2015_03 |
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