HCID 10089559, compound → HCID 9907370, compound

HRID 1271847Notes

Reaction equation

HRID 1271847 reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15]([C:17]1[S:21][C:20]2[CH:22]=[CH:23][C:24]([O:26][CH2:27][CH2:28][CH2:29][N:30]([CH3:32])[CH3:31])=[CH:25][C:19]=2[CH:18]=1)=[O:16])(C)(C)C.NC1C=CC=CC=1NC(C1SC2C=CC(OCCN(C)C)=CC=2C=1)=O>>[NH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15]([C:17]1[S:21][C:20]2[CH:22]=[CH:23][C:24]([O:26][CH2:27][CH2:28][CH2:29][N:30]([CH3:31])[CH3:32])=[CH:25][C:19]=2[CH:18]=1)=[O:16]

Participants

3

Reactant 2

HCID 10089559HCID 10089559, compoundHCID 69490179HCID 69490179, compound

Product 1

HCID 9907370HCID 9907370, compound

Procedure

was prepared from (2-{[5-(3-Dimethylamino-propoxy)-benzo[b]thiophene-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester (7) in an analogous manner to that described for the preparation of (1) example 1, step 5; white solid, mp. 164–167° C.

Sources & evidence

ORD record
ord-21d1bfe5a5e54fc08153df1f7356a88d
Source dataset
uspto-grants-2007_04
Patent number
US07208491B2

Reaction notes

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