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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849230Generated: October 26, 2026

Benzyl Bromide → 6-(5-Ethyl-1,3,4-thiadiazol-2-ylthiomethyl)-4-morpholino-2-[6-(2-propenyloxycarbonylamino)-2-pyridylmethylamino]pyridine

https://huagongshe.com/reaction/849230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl 6-(chloromethyl)pyridine-2-carboxylateHCID 15614003—
Reactant(+/-)-6-[1-(5-Ethyl-1,3,4-thiadiazol-2-ylthio)ethyl]-4-morpholino-2-[3-(2-propenyloxycarbonylamino)benzylamino]pyridineHCID 19369555—
Product6-(5-Ethyl-1,3,4-thiadiazol-2-ylthiomethyl)-4-morpholino-2-[6-(2-propenyloxycarbonylamino)-2-pyridylmethylamino]pyridineHCID 19369722—

Reaction Steps

The above identified compound was obtained as a pale yellow solid in the same manner as in Example 1-(6), Example 4-(2) and (3) and Example 1-(7) except that benzyl bromide was changed to ethyl 6-chloromethylpyridine-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011039
Source datasetuspto-grants-2000_01
ORD IDord-882efe6d3d154f0697354f081212610a
Source noteuspto-grants-2000_01