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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269362Generated: October 30, 2026

1,3,4-Thiadiazol-2-amine → HCID 70085747, compound

https://huagongshe.com/reaction/2269362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,4-Thiadiazol-2-amineHCID 19909—
ReactantBoc-Lys(Z)-OHHCID 2724765—
SolventDichloromethaneHCID 6344—
ProductHCID 70085747HCID 7008574761%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (2S)-6-benzyloxycarbonylamino-2-tert-butoxycarbonylaminohexanoic acid (1.09 g, 2.87 mmol) in dichloromethane (5 mL) is added 1,1-carbonyldiimidazole (0.47 g, 2.87 mmol). The resulting solution is stirred at 25° C. for 1 h and 2-amino-1,3,4-thiadiazole (0.29 g, 2.87 mmol) is added and the reaction is stirred for an additional 18 h. The mixture is diluted with dichloromethane (60 mL) and washed with 1 M aqueous sodium carbonate solution. The organic layer is dried over anhydrous magnesium sulfate, concentrated in vacuo, and purified by silica gel chromatography (elution with 1:1 EtOAc-hexanes) to provide (2S)-6-benzyloxycarbonylamino-2-tert-butoxycarbonylaminohexanoic acid 1,3,4-thiadiazol-2-ylamide as a foam (0.81 g, 61% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329400B1
Source datasetuspto-grants-2001_12
ORD IDord-7f102f34a43041988f9c3a6eb7a18721
Source noteuspto-grants-2001_12