Isocyanate → HCID 178507143, compound

HRID 32484Notes

Reaction equation

HRID 32484 reaction equation
[CH2:1]1[C:9]2[C:4](=[CH:5][C:6]([N:10]=[C:11]=[O:12])=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.[N-]=C=O.[NH2:16][C:17]1[N:22]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([NH2:29])[CH:24]=2)[CH2:21][N:20]=[C:19]2[O:30][CH:31]=[CH:32][C:18]=12>>[NH2:16][C:17]1[N:22]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([NH:29][C:11]([NH:10][C:6]3[CH:5]=[C:4]4[C:9](=[CH:8][CH:7]=3)[CH2:1][CH2:2][CH2:3]4)=[O:12])[CH:24]=2)[CH2:21][N:20]=[C:19]2[O:30][CH:31]=[CH:32][C:18]=12

Participants

4

Reactant 3

HCID 105034IsocyanateHCID 50036815-Indanyl isocyanateHCID 178507142HCID 178507142, compound

Product 1

HCID 178507143HCID 178507143, compound

Procedure

The compound was prepared following the procedure described in Example 232(b), using 5-indanyl isocyanate as the isocyanate of choice, and 4-Amino-3-(3-aminophenyl)furo[2,3-d]pyrimidine (10) as the diamine of choice. MS(ES) m/e 386 [M+H]+.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-a8e1eeb6f84c4593a536d2c6952de70b
Source dataset
uspto-grants-2008_09
Patent number
US07427623B2

Reaction notes

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