Isocyanate → HCID 68906100, compound

HRID 1785642Notes

Reaction equation

HRID 1785642 reaction equation
Cl[C:2]1[CH:20]=[CH:19][C:5]([CH:6](OC2CNC2)[C:7]2C=CC(Cl)=CC=2)=[CH:4][CH:3]=1.[N-]=C=O.Cl[C:25]1[CH:50]=[C:49]([Cl:51])[CH:48]=[CH:47][C:26]=1[CH:27]([O:35][CH:36]1[CH2:39][N:38]([C:40]([NH:42]C(C)(C)C)=[O:41])[CH2:37]1)[C:28]1[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][CH:29]=1>>[Cl:34][C:31]1[CH:30]=[CH:29][C:28]([CH:27]([O:35][CH:36]2[CH2:39][N:38]([C:40]([NH:42][CH2:7][CH2:6][C:5]3[CH:19]=[CH:20][CH:2]=[CH:3][CH:4]=3)=[O:41])[CH2:37]2)[C:26]2[CH:25]=[CH:50][C:49]([Cl:51])=[CH:48][CH:47]=2)=[CH:33][CH:32]=1

Participants

4

Reactant 3

HCID 105034IsocyanateHCID 114420773-(2,4,4'-trichlorobenzhydryloxy)-N-(tert-butyl)azetidine-1-carboxamideHCID 689061393-(4,4'-Dichlorobenzhydryloxy)azetidine

Product 1

HCID 68906100HCID 68906100, compound

Procedure

This material was prepared from 3-(4,4′-dichlorobenzhydryloxy)azetidine (36) and the corresponding commercially available isocyanate, using the procedure described for compound (5).

Sources & evidence

ORD record
ord-15fc2f8659ec4a458b3042b4e20c5f49
Source dataset
uspto-grants-2009_03
Patent number
US07504522B2

Reaction notes

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