3-(naphthalene-2-sulfonamido)-3-phenylpropionic Acid → HCID 68926906, compound

HRID 32060Notes

Reaction equation

HRID 32060 reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[S:11]([NH:14][CH:15]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:16][C:17](O)=[O:18])(=[O:13])=[O:12].[NH2:26][CH:27]1[C:35]2[C:30](=[CH:31][C:32]([C:36]#[N:37])=[CH:33][CH:34]=2)[CH2:29][CH2:28]1>>[C:36]([C:32]1[CH:31]=[C:30]2[C:35](=[CH:34][CH:33]=1)[CH:27]([NH:26][C:17](=[O:18])[CH2:16][CH:15]([NH:14][S:11]([C:2]1[CH:3]=[CH:4][C:9]3[C:10](=[CH:5][CH:6]=[CH:7][CH:8]=3)[CH:1]=1)(=[O:13])=[O:12])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:28][CH2:29]2)#[N:37]

Participants

3

Reactant 2

HCID 36326413-(naphthalene-2-sulfonamido)-3-phenylpropionic AcidHCID 552949751-amino-2,3-dihydro-1H-indene-5-carbonitrile

Product 1

HCID 68926906HCID 68926906, compound

Procedure

The title compound was prepared from 3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionic acid [Example 1, Step F] and 1-amino-indan-5-carbonitrile (Step E), using essentially the same procedure described in Example 1, Step F, yielding a white solid. MS (ESI) m/z 496 (M+H)+.

Workup

  1. customyielding a white solid

Sources & evidence

ORD record
ord-1cd98a8976ef45e3b987bcd35e82a096
Source dataset
uspto-grants-2008_09
Patent number
US07425631B2

Reaction notes

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