Benzenesulfonyl chloride → HCID 68596879, compound

HRID 1890381Notes

Reaction equation

[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH:10]3[CH2:13][N:12]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:11]3)=[CH:7][CH:8]=2)[CH:3]=[N:2]1.[C:21]1([S:27](Cl)(=[O:29])=[O:28])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:21]1([S:27]([N:1]2[C:9]3[C:4](=[CH:5][C:6]([CH:10]4[CH2:13][N:12]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:11]4)=[CH:7][CH:8]=3)[CH:3]=[N:2]2)(=[O:29])=[O:28])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

Participants

Reactant 2

HCID 7369Benzenesulfonyl chloride

HCID 68597910HCID 68597910, compound

Product 1

HCID 68596879HCID 68596879, compound

Procedure

This compound was prepared from tert-butyl 3-(1H-indazol-5-yl)azetidine-1-carboxylate and benzenesulfonylchloride by the method outlined under 44.c).

Sources & evidence

ORD record: ord-a34afe88385e4fe48ff481997fa0322c
Source dataset: uspto-grants-2013_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08507469B2

Reaction notes

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