Cyclopentylamine → HCID 67559013, compound
Reaction equation
Cl[S:2][C:3]1C=CC=C[C:4]=1[C:5](Cl)=[O:6].[CH:12]1([NH2:17])[CH2:16][CH2:15][CH2:14][CH2:13]1>>[CH:12]1([N:17]2[C:5](=[O:6])[CH2:4][CH2:3][S:2]2)[CH2:16][CH2:15][CH2:14][CH2:13]1Participants
3
Procedure
This was prepared in analogous manner to that described in Example 17 except using 2-chlorosulphenylbenzoyl chloride (5.175 parts, 0.025M) and cyclopentylamine (8.52 parts, 0.1M ex Aldrich). The product was obtained as a yellow oil (5.9 parts) which was recrystallised form hexane mp 87-88° C.
Workup
- customThis was prepared in analogous manner to that
- customThe product was obtained as a yellow oil (5.9 parts) which
- customwas recrystallised form hexane mp 87-88° C.
Sources & evidence
- ORD record
- ord-cd7e46cb3de944249bea85bf2a54112b
- Source dataset
- uspto-grants-1999_12
- Patent number
- US06005032
Reaction notes
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