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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769073Generated: October 31, 2026

Triethylamine → HCID 14950485, compound

https://huagongshe.com/reaction/1769073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 14950483HCID 14950483—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14950485HCID 14950485—

Reaction Steps

Triethylamine (2.2 ml) and methanesulphonyl chloride (1.24 ml) were added to a solution of compound B (10.0 g) in dichloromethane (150 ml). The solution was left to stand for 20 hours and then diluted with water (150 ml). The organic phase was separated, washed with saturated sodium chloride solution (150 ml), and dried (MgSO4). Volatile material was removed by evaporation and the residue was purified by flash chromatography, eluting with a mixture of methanol and dichlormethane (1:19 v/v) to give 3-chloromethyl-2,6-dimethyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]pyridine (C) (8.5 g), as a white solid, m.p. 110°-112° C.; NMR (d6 -DMSO/d4 -acetic acid): 2.5(s,3H), 2.65(s,3H), 4.75(s,2H), 5.45(s,2H), 6.9-7.9 (complex m,24H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380730
Source datasetuspto-grants-1995_01
ORD IDord-988707c374bb43db9be2cbadc0105971
Source noteuspto-grants-1995_01