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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641297Generated: October 30, 2026

3-(Trifluoromethyl)benzenesulfonyl chloride → HCID 66789933, compound

https://huagongshe.com/reaction/641297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
ReactantHCID 66788850HCID 66788850—
ReactantHCID 66789221HCID 66789221—
ProductHCID 66789933HCID 66789933—

Reaction Steps

2-Fluoro-4-{[4-(3-trifluoromethyl-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-benzoic acid, MS (ISP): m/e=523.0 (M−H), was prepared as described for example 14, steps 1 to 8. Step 4 was performed using 4-amino-2-fluoro-benzoic acid ethyl ester, yielding 4-(4-benzyloxy-3-nitro-benzoylamino)-2-fluoro-benzoic acid ethyl ester, which was reduced to 4-(3-amino-4-hydroxy-benzoylamino)-2-fluoro-benzoic acid methyl ester in step 5 and cyclized to 4-[(3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl)-amino]-2-fluoro-benzoic acid ethyl ester in step 6. Step 7 was performed using 3-trifluoromethyl-benzenesulfonyl chloride and yielded 2-fluoro-4-{[4-(3-trifluoromethyl-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-benzoic acid ethyl ester, which was hydrolyzed in step 8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696200B2
Source datasetuspto-grants-2010_04
ORD IDord-d8efb2e8c6ce45b78ca352e69670948f
Source noteuspto-grants-2010_04