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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078790Generated: November 2, 2026

Acetic Anhydride → N-(2-(4-(2-chlorophenyl)-4H-1,2,4-triazol-3-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-8-yl)acetamide

https://huagongshe.com/reaction/2078790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 66899984HCID 66899984—
SolventDichloromethaneHCID 6344—
ProductN-(2-(4-(2-chlorophenyl)-4H-1,2,4-triazol-3-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-8-yl)acetamideHCID 4424216639%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(4-(2-chlorophenyl)-4H-1,2,4-triazol-3-yl)-4,5-dihydro-benzo[b]thieno[2,3-d]oxepin-8-amine HCl salt (0.2 g, 0.464 mmol) in 10 ml of dried DCM was added TEA (0.32 mL, 2.3 mmol). The mixture was stirred at 0° C. for 20 min and 0.2 ml of acetic anhydride was added. After stirred for 10 min, the solution was quenched with water and evaporated to the crude product, which was purified by preparative TLC to give 115 (80 mg, 39%). 1H NMR (DMSO-d6, 400 MHz): δ 10.02 (s, 1H), 8.81 (s, 1H), 7.79-7.15 (m, 7H), 6.54 (s, 1H), 4.16 (t, J=4.8 Hz, 2H), 2.95 (t, J=4.8 Hz, 2H), 1.99 (s, 3H). MS: (ESI+) 437.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928248B2
Source datasetuspto-grants-2011_04
ORD IDord-e84b61af5f3e403892083c0eeb3bd975
Source noteuspto-grants-2011_04