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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013189Generated: October 25, 2026

2-chloro-N-(4-fluorophenyl)acetamide → (3-{2-[(4-Fluoro-phenylcarbamoyl)-methyl]-1,1-dioxo-2,3-dihydro-1H-1lambda6-benzo[d]isothiazol-3-yl}-2-methyl-indol-1-yl)-acetic acid

https://huagongshe.com/reaction/1013189

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-N-(4-fluorophenyl)acetamideHCID 532065—
Reactant[3-(1,1-Dioxo-2,3-dihydro-1h-1lambda6-benzo[d]isothiazol-3-yl)-2-methyl-indol-1-yl]-acetic acid tert-butyl esterHCID 67317115—
Product(3-{2-[(4-Fluoro-phenylcarbamoyl)-methyl]-1,1-dioxo-2,3-dihydro-1H-1lambda6-benzo[d]isothiazol-3-yl}-2-methyl-indol-1-yl)-acetic acidHCID 59753842—

Reaction Steps

The title compound was prepared by the method described for example 14 using the product from example 3, step c) and alpha-chloro-4-fluoroacetanilide. 1H NMR (DMSO-d6) δ 8.06-8.03 (m, 1H), 7.70-7.62 (m, 2H), 7.51-7.46 (m, 2H), 7.39 (d, J=8.4 Hz, 1H), 7.17-7.13 (m, 2H), 7.02 (t, J=8.1 Hz, 1H), 6.80 (t, J=7.5 Hz, 1H), 6.72 (bs, 1H), 6.55 (s, 1H), 5.00 (s, 2H), 4.15 (d, J=17.4 Hz, 1H), 3.40 (d, J=17.4 Hz, 1H), 2.39 (s, 3H); MS: ESI (negative): 506 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981912B2
Source datasetuspto-grants-2011_07
ORD IDord-d86dc904227b4107ad3fe4f28c8f15ca
Source noteuspto-grants-2011_07