HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879394Generated: October 31, 2026
Sodium Hydroxide → (S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-(1,3-dimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridine-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetic acid
https://huagongshe.com/reaction/879394
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-(1,3-dimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridine-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetate | HCID 86700199 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | (S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-(1,3-dimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridine-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetic acid | HCID 86700201 | — |
Reaction Steps
To a solution of (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-(1,3-dimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridine-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetate: (28 mg, 0.044 mmol) in THF/CH3OH (1.0 mL/1.0 mL) was added 2N NaOH (0.22 mL, 0.44 mmol). The reaction mixture was heated at 50° C. for 2 h and the crude was purified by reverse phase HPLC, eluting by 0-100% acetonitrile in H2O with 0.1% TFA to give the product. LCMS-ESI+: calc'd for C34H31ClN4O3S: 611.2 (M+H+); Found: 611.2 (M+H+); 1H NMR (400 MHz, CD3OD) δ 9.11 (s, 1H), 8.79 (d, J=5.6 Hz, 1H), 8.18-7.64 (m, 8H), 7.32 (s, 1H), 5.29 (s, 1H), 3.96 (s, 3H), 2.66 (s, 3H), 2.34 (s, 3H), 0.99 (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-e75cf6071caf41efa315aa0d7b26d55d |
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| Source note | uspto-grants-2015_03 |
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