HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641409Generated: October 30, 2026
1H-Benzotriazole-1-methanol → HCID 59257892, compound
https://huagongshe.com/reaction/641409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Benzotriazole-1-methanol | HCID 224169 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one | HCID 59166722 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59257892 | HCID 59257892 | — |
Reaction Steps
A mixture of (−)-5-amino-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (154 mg, 0.613 mmol, described in Intermediate 3) and 1-(hydroxymethyl)benzotriazole (93 mg, 0.625 mmol) in EtOH (2 mL) and DMF (0.2 mL) was heated at reflux for 4 h, then concentrated to dryness under reduced pressure. The residue was resuspended in THF (3 mL) and sodium borohydride (40 mg, 1.05 mmol) was added. The resulting mixture was heated to 70° C. for 6 h then quenched with H2O (50 mL) and extracted with EtOAc (50 mL). The organic extract was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 80:20, to give the title compound, which was of sufficient purity for use in the next step. MS: m/z=266 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07696192B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-543b3ec0e0a641a0ae8ea7f87ba85918 |
|---|
| Source note | uspto-grants-2010_04 |
|---|