1-Pyrrolidinesulfonyl chloride → HCID 44218873, compound

HRID 1928772Notes

Reaction equation

HRID 1928772 reaction equation
[N:1]1([S:6](Cl)(=[O:8])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.[C@H:10]1([NH:19][C:20]2[CH:29]=[CH:28][C:27]3[C:22](=[CH:23][CH:24]=[C:25]([NH2:30])[CH:26]=3)[N:21]=2)[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:12][CH2:11]1>>[C@H:10]1([NH:19][C:20]2[CH:29]=[CH:28][C:27]3[C:22](=[CH:23][CH:24]=[C:25]([NH:30][S:6]([N:1]4[CH2:5][CH2:4][CH2:3][CH2:2]4)(=[O:8])=[O:7])[CH:26]=3)[N:21]=2)[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:12][CH2:11]1

Participants

3

Procedure

The title compound was prepared in accordance with the general method described in example 66 from pyrrolidine-1-sulfonyl chloride and (R)—N2-indan-1-yl-quinoline-2,6-diamine; MS: m/e=409.6 (M+H+).

Sources & evidence

ORD record
ord-f40f9003f7c344848298cd499e12f3eb
Source dataset
uspto-grants-2012_05
Patent number
US08183380B2

Reaction notes

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