Phenethylsulfamide → 7-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-4,7-diaza-spiro[2.5]octane-4-sulfonic acid phenethyl-amide

HRID 589946Notes

Reaction equation

HRID 589946 reaction equation
[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[C:4]([N:10]2[CH2:17][C:14]3([CH2:16][CH2:15]3)[N:13]([S:18]([NH2:21])(=[O:20])=[O:19])[CH2:12][CH2:11]2)=[N:3][CH:2]=1.S(N[CH2:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)(=O)(=O)N>>[CH2:27]([NH:21][S:18]([N:13]1[CH2:12][CH2:11][N:10]([C:4]2[C:5]3[CH:9]=[CH:8][NH:7][C:6]=3[N:1]=[CH:2][N:3]=2)[CH2:17][C:14]21[CH2:16][CH2:15]2)(=[O:20])=[O:19])[CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1

Participants

3

Reactant 2

HCID 12827PhenethylsulfamideHCID 574100947-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-4,7-diaza-spiro[2.5]octane-4-sulfonic acid amide

Product 1

HCID 574100967-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-4,7-diaza-spiro[2.5]octane-4-sulfonic acid phenethyl-amide

Procedure

Prepared in a way similar to intermediate 1, using 2-(sulfamoylamino)-ethylbenzene instead of sulfamide.

Sources & evidence

ORD record
ord-1503738b19a24881a2e1067cc1d576fd
Source dataset
uspto-grants-2016_01
Patent number
US09233964B2

Reaction notes

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