Isocyanate → HCID 178436418, compound

HRID 32493Notes

Reaction equation

HRID 32493 reaction equation
[NH2:1][C:2]1[N:7]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][CH3:15])=[CH:10][CH:9]=2)[CH2:6][N:5]=[C:4]2[S:16][CH:17]=[CH:18][C:3]=12.[CH2:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1N=C=O)[CH3:20].[N-:30]=[C:31]=[O:32]>>[NH2:1][C:2]1[N:7]([C:8]2[CH:9]=[CH:10][C:11]([N:14]([C:31]([NH:30][C:23]3[CH:24]=[CH:25][CH:26]=[C:21]([CH2:19][CH3:20])[CH:22]=3)=[O:32])[CH3:15])=[CH:12][CH:13]=2)[CH2:6][N:5]=[C:4]2[S:16][CH:17]=[CH:18][C:3]=12

Participants

4

Reactant 3

HCID 105034IsocyanateHCID 5834862-Ethylphenyl isocyanateHCID 178482193HCID 178482193, compound

Product 1

HCID 178436418HCID 178436418, compound

Procedure

The compound was prepared following the procedure described in Example 429, substituting 4-amino-3-(4-(methylamino)phenyl)-thieno[2,3-d]pyrimidine as the amine and using 2-ethyl-phenyl isocyanate as the isocyanate of choice. MH+=404.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-7b618d09fbb341909742f5d50cbd899a
Source dataset
uspto-grants-2008_09
Patent number
US07427623B2

Reaction notes

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