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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633491Generated: October 30, 2026

Sodium borohydride → 1,1-Dimethylethyl (6-{[6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-1,3-benzothiazol-2-yl)carbamate

https://huagongshe.com/reaction/633491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Chloro-6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazineHCID 21822190—
Reactant1,1-Dimethylethyl (6-sulphanyl-1,3-benzothiazol-2-yl)carbamateHCID 46853772—
SolventEthanolHCID 702—
Product1,1-Dimethylethyl (6-{[6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-1,3-benzothiazol-2-yl)carbamateHCID 8670700742.5%

Reaction Steps

68 mg of sodium borohydride are added to a mixture of 430 mg of 3-chloro-6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazine and 510 mg of 1,1-dimethylethyl (6-sulphanyl-1,3-benzothiazol-2-yl)carbamate in 9 cm3 of degassed ethanol and then the reaction is refluxed for 23 h. The suspension is left at 20° C. overnight and is then concentrated to dryness under vacuum. The product is chromatographed by solid deposit on a Merck cartridge of 70 g of silica 15-40 μm, elution being carried out with a gradient of 100% dichloromethane to 95/5 dichloromethane/methanol. 370 mg of 1,1-dimethylethyl (6-{[6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-1,3-benzothiazol-2-yl)carbamate are thus obtained in the form of a white solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321777B2
Source datasetuspto-grants-2016_04
ORD IDord-5adcb00a82e14d5ba4b522aa9aa1227a
Source noteuspto-grants-2016_04