HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510319Generated: October 26, 2026
Hydrochloric Acid → 4-(6-((S)-tert-butoxy(carboxy)methyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-2-ylamino)-3-(1-methyl-1H-indazol-5-yl)butanoic acid
https://huagongshe.com/reaction/510319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(4-(1-methyl-1H-indazol-5-yl)-2-oxopyrrolidin-1-yl)benzo[d]thiazol-6-yl)acetate | HCID 86699849 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 4-(6-((S)-tert-butoxy(carboxy)methyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-2-ylamino)-3-(1-methyl-1H-indazol-5-yl)butanoic acid | HCID 86699850 | — |
Reaction Steps
To a solution of (2S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(4-(1-methyl-1H-indazol-5-yl)-2-oxopyrrolidin-1-yl)benzo[d]thiazol-6-yl)acetate (5 mg) in THF/MeOH (0.5 mL/0.5 mL) was added sodium hydroxide solution (1.0 N, 0.5 mL). The mixture was stirred at 25° C. for 2 hours and heated at 50° C. for 16 hours. The mixture was cooled and neutralized with 0.1 N hydrochloric acid until pH=5. The reaction mixture was freeze-dried and used for next step without further purification. LCMS-ESI+: calc'd for C32H33ClN4O5S: 621.2 (M+H+); Found: 621.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096586B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-7a4d3f4854d748bd83d38d6d80b749b1 |
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| Source note | uspto-grants-2015_08 |
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