HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656830Generated: October 28, 2026
Hydrochloric Acid → HCID 67174106, compound
https://huagongshe.com/reaction/656830
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86629724 | HCID 86629724 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67174106 | HCID 67174106 | — |
Reaction Steps
A solution of tert-butyl ((2S)-6-nitro-2′-oxo-1′-{[2-(trimethylsilyl)ethoxy]methyl}-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-yl)acetate from Step C (2.01 g, 3.83 mmol) in MeOH (25 mL) was saturated with HCl (g) and stood at ambient temperature for 18 h. The mixture was concentrated to dryness in vacuo, then redissolved in MeOH (25 mL). This stirred solution was adjusted to pH 10 with 10 N NaOH and ethylene diamine (0.26 mL, 3.83 mmol) was added. The resulting mixture was stirred for 3 h, then concentrated to dryness in vacuo. The residue was dissolved in THF (25 mL) and 1 N NaOH (25 mL, 25 mmol) was added. The mixture was stirred at ambient temperature for 18 h, then the THF was removed under reduced pressure. The residual mixture was partitioned between saturated aqueous NaHCO3 (50 mL) and EtOAc (100 mL). The organic layer was discarded and the aqueous layer was adjusted to pH 2 with aqueous HCl, then extracted with EtOAc (3×200 mL). The combined organic layers were dried over Na2 SO4, filtered, and concentrated under reduced pressure to give the title compound. MS: m/z=340 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071772B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-5978ec9ace4542758e88559b5a690091 |
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| Source note | uspto-grants-2011_12 |
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