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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10997Generated: October 25, 2026

p-(Trifluoromethoxy)benzenesulphonyl chloride → CID 145857204

https://huagongshe.com/reaction/10997

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)benzenesulphonyl chlorideHCID 523102—
Reactanttert-butyl N-[4-[[[(6S)-3-(methanesulfonamido)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamateHCID 145857232—
Reactanttert-butyl N-[4-[[[(6S)-3-(diethylamino)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamateHCID 145857233—
ProductCID 145857204HCID 14585720441.6%

Reaction Steps

Following a procedure similar to that for the preparation of 16a, intermediate 3a (50 mg, 0.117 mmol) and 4-(trifluoromethoxy)benzene sulfonyl chloride (39.6 mg, 0.152 mmol) yielded 31.7 mg (41.6%) of 33a. MS (ESI) 651.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094783B2
Source datasetuspto-grants-2006_08
ORD IDord-4c34701dba374642a831397d727793bd
Source noteuspto-grants-2006_08