HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506177Generated: November 4, 2026
Hydrochloric Acid → HCID 68463421, compound
https://huagongshe.com/reaction/506177
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | tert-butyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamate | HCID 2733675 | — |
| Reactant | HCID 68463685 | HCID 68463685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68463421 | HCID 68463421 | 30% |
Reaction Steps
To a suspension of 5-(4-hydroxyphenyl)-4-(1H-indol-4-ylamino)nicotinonitrile 225 (100 mg, 0.31 mmol), tert-butyl (1S)-1-benzyl-2-hydroxyethylcarbamate (77 mg, 0.31 mmol), and Ph3P (97 mg, 0.37 mmol) in THF (2.0 mL) was added diethyl azodicarboxylate (64 mg, 0.37 mmol) via a syringe over 6 min. The resulting mixture was stirred at r.t. for 21 h and treated with concentrated HCl (˜200 mg). After heating at 60° C. for one h, the reaction mixture was partitioned between saturated NaHCO3 and CH2Cl2. The combined organics were dried over Na2SO4, concentrated and purified by silica gel flash column chromatography (eluting with 4% MeOH/CH2Cl2) to give 42 mg (30%) of 5-(4-{[(2S)-2-amino-3-phenylpropyl]oxy}phenyl)-4-(1H-indol-4-ylamino)nicotinonitrile 226 as a white solid. MS: 460.4 (M+H); melting range: 83-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781591B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-fb06c6b68cda42dc894c453977d34041 |
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| Source note | uspto-grants-2010_08 |
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