Methyl Isocyanate → HCID 131723919, compound
Reaction equation
[O:1]1[CH2:5][CH2:4][C@@H:3]([NH:6][C:7]2[N:15]=[CH:14][N:13]=[C:12]3[C:8]=2[N:9]=[CH:10][N:11]3[C@@H:16]2[O:20][C@H:19]([CH2:21][S:22][C:23]([NH:25][CH3:26])=[O:24])[C@@H:18]([OH:27])[C@H:17]2[OH:28])[CH2:2]1.CN=C=O>>[O:1]1[CH2:5][CH2:4][C@@H:3]([NH:6][C:7]2[N:15]=[CH:14][N:13]=[C:12]3[C:8]=2[N:9]=[CH:10][N:11]3[C@@H:16]2[O:20][C@H:19]([CH2:21][S:22][C:23]([NH:25][CH:26]3[CH2:5][CH2:4][CH2:3][CH2:2]3)=[O:24])[C@@H:18]([OH:27])[C@H:17]2[OH:28])[CH2:2]1Participants
3
Procedure
Compound 73 was prepared in the manner of compound 22 by substituting cyclopentyl isocyanate for methyl isocyanate [MS 465.2 (M+1)].
Sources & evidence
- ORD record
- ord-e797670c74904210a056f4496ded8e1e
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06576620B2
Reaction notes
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