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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708215Generated: October 26, 2026

2-chloro-N-(1-methylethyl)acetamide → N-Isopropyl-2-{3-[2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-azetidin-1-yl}-acetamide

https://huagongshe.com/reaction/708215

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-N-(1-methylethyl)acetamideHCID 76171—
Reactant2-{3-[2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-azetidin-1-yl}-acetamideHCID 58204244—
Reactant8-azetidin-3-yl-2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene TFA saltHCID 86652316—
ProductN-Isopropyl-2-{3-[2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-azetidin-1-yl}-acetamideHCID 67050512—

Reaction Steps

Following the procedure of 319, a suspension of 8-azetidin-3-yl-2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene TFA salt 235 (200 mg, 0.42 mmol) and N-isopropyl-2-chloroacetamide gave 470 isolated as a yellow solid (91 mg, 26%). LCMS: RT=3.31 min, [M+H]+=467. 1H NMR δ (ppm) (DMSO-d6): 8.26 (1H, d, J=8.18 Hz), 8.05 (1H, s), 7.40 (1H, d, J=8.06 Hz), 7.17 (1H, dd, J=8.24, 1.83 Hz), 6.99 (1H, d, J=1.78 Hz), 5.83-5.73 (1H, m), 4.35-4.29 (2H, m), 3.86-3.80 (1H, m), 3.69-3.58 (3H, m), 3.41-3.35 (2H, m), 3.18 (2H, d, J=6.73 Hz), 3.00 (2H, s), 1.50 (6H, d, J=6.59 Hz), 1.03 (6H, d, J=6.59 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175009B2
Source datasetuspto-grants-2015_11
ORD IDord-8ba97e19f695470aa1bfb71e37a0f9ff
Source noteuspto-grants-2015_11