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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386485Generated: October 31, 2026

HCID 21717622, compound → HCID 178439175, compound

https://huagongshe.com/reaction/1386485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21717622HCID 21717622—
ReactantHCID 21717629HCID 21717629—
ReactantHCID 178509300HCID 178509300—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178439175HCID 17843917512%

Reaction Steps

1 equivalent of N,N′-carbonyldi-imidazole (Aldrich, 0.46 g, 0.29 mmol) is added, at ambient temperature to a solution of acid (E) 4-[1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-2-propenyl]benzoic acid (0.10 g, 0.29 mmol) in 5 ml of anhydrous THF. Half an hour later, 1 equivalent of 5-aminotetrazole monohydrate (Aldrich, 0.30 g, 0.29 mmol) is added. The magnetic stirring is continued for 15 hours 30 minutes. A white precipitate forms in the reaction medium. The mixture is evaporated to dryness and 10 ml of HCl is added. The solution is filtered and the filtrate washed with water and with methanol. After drying one night in a desiccator (with P2O5), 15 mg of a white solid is obtained the compound (E) 4-[1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-2-propenyl]-N-(tetrazol-5-yl)-benzamide (compound CB73364) (yield=12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265423B1
Source datasetuspto-grants-2001_07
ORD IDord-e0f00d010d03442697b2a5016188d27f
Source noteuspto-grants-2001_07