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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861007Generated: October 27, 2026

Sodium borohydride → HCID 10436965, compound

https://huagongshe.com/reaction/861007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69374948HCID 69374948—
ReactantHCID 178418689HCID 178418689—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 10436965HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153968B2
Source datasetuspto-grants-2006_12
ORD IDord-955bc16ddf28410c8d9e47a14887e4bc
Source noteuspto-grants-2006_12