HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861007Generated: October 27, 2026
Sodium borohydride → HCID 10436965, compound
https://huagongshe.com/reaction/861007
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 69374948 | HCID 69374948 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 10436965 | HCID 10436965 | — |
Reaction Steps
To a solution of difluoro-(5-{3-[6-(1-methanesulfonyl-1-methyl-ethyl)-quinolin-8-yl]-phenyl}-pyridin-3-ylsulfanyl)-acetic acid ethyl ester from Step 1 (1.0 eq.) in CH2Cl2 (0.2M) at −78° C. was added MeMgBr (3.0 eq.; 3.0M in Et2O). The mixture was warmed to rt, stirred for 12 h, poured in saturated aqueous NH4Cl and extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was dissolved in EtOH (0.2M) then NaBH4 (3.0 eq.) was added. The mixture was stirred for 2 h, poured in saturated aqueous NH4Cl and extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated. Flash chromatography (Hex:EtOAc; 1:9) afforded the title compound as a white solid. 1H NMR (400 MHz, acetone-d6): δ 9.04 (d, 1H), 8.97 (dd, 1H), 8.75 (d, 1H), 8.50 (dd, 1H), 8.35–8.34 (m, 2H), 8.26 (d, 1H), 8.13 (s, 1H), 7.85 (dt, 1H), 7.82 (dt, 1H), 7.68 (t, 1H), 7.61 (dd, 1H), 5.15 (d, 1H), 4.20 (m, 1H), 2.76 (s, 3H), 2.03 (s, 6H), 1.37 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153968B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-955bc16ddf28410c8d9e47a14887e4bc |
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| Source note | uspto-grants-2006_12 |
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