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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736336Generated: October 30, 2026

2-Chlorobenzenesulfonyl chloride → N-[5-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-3-yl]-2-chloro-benze nesulfonamide

https://huagongshe.com/reaction/736336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantHCID 68902717HCID 68902717—
Reactant(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-(5-amino-pyridin-3-yl)-methanoneHCID 68903795—
ProductN-[5-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-3-yl]-2-chloro-benze nesulfonamideHCID 68904444—

Reaction Steps

The title compound was prepared from 2-Chloro-benzenesulfonyl chloride (19.6 mg, 0.093 mmol) and (4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-(5-amino-pyridin-3-yl)-methanone (25 mg, 0.084 mmol) by procedures analogous to those described for the preparation of N-[5-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-pyridin-3-yl]-3,5-difluoro-benzenesulfonamide. MS: 471.2 (MH+); HPLC Rf: 4.71 min. (HPLC method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595325B2
Source datasetuspto-grants-2009_09
ORD IDord-e63e25e0de0c4f3681d43c9ff8e23470
Source noteuspto-grants-2009_09