Isocyanate → HCID 68906238, compound

HRID 1785643Notes

Reaction equation

HRID 1785643 reaction equation
ClC1C=CC([CH:6](OC2CNC2)[C:7]2[CH:12]=[CH:11][C:10](Cl)=[CH:9][CH:8]=2)=CC=1.[N-]=[C:22]=[O:23].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:51][C:49]1[CH:48]=[CH:47][C:26]([CH:27]([O:35][CH:36]2[CH2:39][N:38]([C:40]([NH:42][CH2:6][C:7]3[CH:8]=[CH:9][C:10]([O:23][CH3:22])=[CH:11][CH:12]=3)=[O:41])[CH2:37]2)[C:28]2[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][CH:29]=2)=[CH:25][CH:50]=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 68906238HCID 68906238, 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-42eecf57f25544aea3951e9fcf79ab27
Source dataset
uspto-grants-2009_03
Patent number
US07504522B2

Reaction notes

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