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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685278Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 12096279, compound

https://huagongshe.com/reaction/1685278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-pyrrolo[2,3-b]pyridineHCID 12096278—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12096279HCID 1209627951%

Reaction Steps

Sodium bis(trimethylsilyl)amide (0.2 mL, 1M in THF, 0.23 mmol) was added to a solution of 3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-7-azaindole (24.9 mg, 0.12 mmol) in THF (2.5 mL) at −78° C. and the mixture stirred for 1 h. Benzenesulfonyl chloride (30 μL, 0.24 mmol) was added and the mixture stirred at room temperature for 2 h, prior to quenching with water (4 drops) and silica gel (.about. 1 g). Purification using solid phase extraction tubes (1000 mg silica, eluting with 0-10% 2M methanolic ammonia in dichloromethane) yielded 3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1-benzenesulfonyl-7-azaindole (21.3 mg, 51%, HRMS-FAB+ for C9 H9 N O S: calculated MH+: 354.12762. Found: 354.12896).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148394B2
Source datasetuspto-grants-2012_04
ORD IDord-29c97f0f52434b5b9062f7f14c4f4430
Source noteuspto-grants-2012_04