Hydrochloric Acid → HCID 68928982, compound

HRID 32063Notes

Reaction equation

HRID 32063 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH:8]([NH:12][C:13](=[O:36])[CH2:14][CH:15]([NH:22][S:23]([C:26]1[CH:35]=[CH:34][C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:27]=1)(=[O:25])=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[CH2:7][CH2:6]2)#[N:2].[ClH:37]>>[ClH:37].[NH2:2][CH2:1][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH:8]([NH:12][C:13](=[O:36])[CH2:14][CH:15]([NH:22][S:23]([C:26]1[CH:35]=[CH:34][C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:27]=1)(=[O:25])=[O:24])[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1)[CH2:7][CH2:6]2

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 68926906HCID 68926906, compound

Product 1

HCID 68928982HCID 68928982, compound

Procedure

The title compound was prepared from N-(5-cyano-indan-1-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide yielding the HCl salt as a white solid. MS (ESI) m/z 500 (M+H)+.

Sources & evidence

ORD record
ord-f1556a5cb2464737b62af6bd1a18defb
Source dataset
uspto-grants-2008_09
Patent number
US07425631B2

Reaction notes

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