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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468185Generated: November 2, 2026

Sodium cyanoborohydride → HCID 56967032, compound

https://huagongshe.com/reaction/1468185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 56967031HCID 56967031—
SolventHCID 21906813HCID 21906813—
ProductHCID 56967032HCID 5696703258%

Reaction Steps

Add to a solution of 3-[4-(4-cyano-phenyl)-[1,2,3]triazol-1-ylmethyl]-N—[(R)-6-(2-methoxy-ethylamino)-4,5,6,7-tetrahydro-benzothiazol-2-yl]-benzamide (0.13 g, 0.20 mmol) in 5 mL MeOH formalin (0.3 mL) and sodium cyanoborohydride (51 mg, 0.82 mmol). Stir the mixture at room temperature for 2 h. Add sat. NH4Cl to the mixture to quench any unreacted sodium cyanoborohydride. Concentrate the mixture, concentrate and purify via preparative HPLC to afford 0.06 g, 58% yield of 3-[4-(4-cyano-phenyl)-[1,2,3]triazol-1-ylmethyl]-N-{(R)-6-[(2-methoxy-ethyl)-methyl-amino]-4,5,6,7-tetrahydro-benzothiazol-2-yl}-benzamide. MS, ES+ 528.44 (M+H), rt 5.33 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000154B2
Source datasetuspto-grants-2015_04
ORD IDord-1987597162ef4e368bd27f71bc570065
Source noteuspto-grants-2015_04