HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338374Generated: October 29, 2026
Hydrochloric Acid → 6-chloro-5-[4-(2-oxopyrrolidin-1-yl)phenyl]-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/338374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 6-chloro-5-[4-(2-oxopyrrolidin-1-yl)phenyl]-1H-indole-3-carboxylate | HCID 86698716 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-chloro-5-[4-(2-oxopyrrolidin-1-yl)phenyl]-1H-indole-3-carboxylic acid | HCID 86698717 | 37.6% |
Reaction Steps
To a mixture of methyl 6-chloro-5-[4-(2-oxopyrrolidin-1-yl)phenyl]-1H-indole-3-carboxylate (112 mg, 0.30 mmol) in methanol (3 mL) and water (3 mL) was added sodium hydroxide (36 mg, 0.94 mmol). The reaction mixture was heated at 75° C. and stirred for 48 hours. The mixture was acidified to pH=4 using 1N hydrochloric acid and concentrated to give a brown solid. It was purified by reverse phase HPLC to give the title compound (40 mg, 37% yield) as a pale solid. MS (ES+) 355.1 (M+H)+. 1H NMR (400 MHz, DMSO-d6) δ 12.11 (br. s, 1H), 11.95 (br. s, 1H), 8.07 (s, 1H), 7.95 (s, 1H), 7.75 (d, 2H), 7.62 (s, 1H), 7.43 (d, 2H), 3.89 (t, 2H), 2.53 (m, 2H), 2.09 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889730B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3c949ec7e1074d4b82ae4d42aa7c5154 |
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| Source note | uspto-grants-2014_11 |
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