1,1-Dioxo-1lambda6-thiolane-3-carboxylic acid → HCID 178523620, compound
Reaction equation
Cl.[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([CH:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C@H:19]4[CH2:24][CH2:23][C@H:22]([NH2:25])[CH2:21][CH2:20]4)[CH2:13][CH2:12]3)[C:5]=2[O:4][CH2:3]1.[O:26]=[S:27]1(=[O:35])[CH2:31][CH2:30][CH:29]([C:32](O)=[O:33])[CH2:28]1>>[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([CH:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C@H:19]4[CH2:20][CH2:21][C@H:22]([NH:25][C:32]([CH:29]5[CH2:30][CH2:31][S:27](=[O:35])(=[O:26])[CH2:28]5)=[O:33])[CH2:23][CH2:24]4)[CH2:13][CH2:12]3)[C:5]=2[O:4][CH2:3]1Participants
3
Procedure
The title compound, white solid (21.1 mg, 54.1%), MS (ISP) m/z=477.2 [(M+H)+], was prepared in accordance with the general method of example 1 from Trans-4-[2-(4-Benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexylamine hydrochloride (intermediate A) (30 mg, 0.0818 mmol) and 1,1-Dioxo-tetrahydro-thiophene-3-carboxylic acid.
Sources & evidence
- ORD record
- ord-fd29e354b7f340d58c67529757937f6a
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598357B2
Reaction notes
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