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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536641Generated: October 29, 2026

Ammonia → HCID 58375185, compound

https://huagongshe.com/reaction/536641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 58375292HCID 58375292—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 58375185HCID 58375185—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Trifluoromethanesulfonic anhydride (0.77 mL) is added to a solution of benzothiazol-6-yl-(8-hydroxy-6-methyl-1,2,5,6-tetrahydro-4H-2,6-methano-benzo[d]azocin-3-yl)-methanone (1.24 g; for synthesis see Example 92), triethylamine (3.4 mL), and 4-dimethylaminopyridine (10 mg) in dichloromethane (12 mL) chilled to −10° C. under argon atmosphere. The solution is stirred at ca. −5° C. for 30 min and then at room temperature overnight. The reaction solution is added to ice-cold water and then concentrated aqueous ammonia solution is added. The resulting mixture is extracted with dichloromethane, the combined organic extracts are washed with water and dried (MgSO4). The solvent is removed under reduced pressure to give the crude product that is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859580B2
Source datasetuspto-grants-2014_10
ORD IDord-f8ed1bbcf23c4b06b2a9544156e6e801
Source noteuspto-grants-2014_10