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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238976Generated: October 30, 2026

5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chloride → Tert-butyl 3-(3-(5-chloro-3-methylbenzo[b]thiophene-2-sulfonamido)phenyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/238976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chlorideHCID 2735756—
ReactantTERT-BUTYL 3-(3-AMINOPHENYL)AZETIDINE-1-CARBOXYLATEHCID 46941930—
ProductTert-butyl 3-(3-(5-chloro-3-methylbenzo[b]thiophene-2-sulfonamido)phenyl)azetidine-1-carboxylateHCID 6895029371%

Reaction Steps

Following the same procedure as described in Example 1.7, tert-butyl 3-(3-aminophenyl)azetidine-1-carboxylate (100 mg, 0.40 mmol) was coupled with 5-chloro-3-methylbenzo[b]thiophene-2-sulfonyl chloride (118 mg, 0.42 mmol) to give tert-butyl 3-(3-(5-chloro-3-methylbenzo[b]thiophene-2-sulfonamido)phenyl)azetidine-1-carboxylate (140 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642642B2
Source datasetuspto-grants-2014_02
ORD IDord-f96f5bc2603e428595b48c08348382b4
Source noteuspto-grants-2014_02