5-Amino-1-piperidin-1-yl-pentan-2-ol → HCID 10029921, compound

HRID 750609Notes

Reaction equation

HRID 750609 reaction equation
C1(O[C:8](=[O:30])[NH:9][C:10]2[S:14][N:13]=[C:12]([O:15][CH2:16][C:17]3[C:22]([F:23])=[CH:21][C:20]([CH3:24])=[C:19]([F:25])[C:18]=3[F:26])[C:11]=2[C:27](=[O:29])[NH2:28])C=CC=CC=1.[NH2:31][CH2:32][CH2:33][CH2:34][CH:35]([OH:43])[CH2:36][N:37]1[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38]1>>[OH:43][CH:35]([CH2:36][N:37]1[CH2:38][CH2:39][CH2:40][CH2:41][CH2:42]1)[CH2:34][CH2:33][CH2:32][NH:31][C:8](=[O:30])[NH:9][C:10]1[S:14][N:13]=[C:12]([O:15][CH2:16][C:17]2[C:22]([F:23])=[CH:21][C:20]([CH3:24])=[C:19]([F:25])[C:18]=2[F:26])[C:11]=1[C:27]([NH2:28])=[O:29]

Participants

3

Reactant 2

HCID 185499355-Amino-1-piperidin-1-yl-pentan-2-olHCID 54053016[4-Carbamoyl-3-(2,3,6-trifluoro-4-methyl-benzyloxy)-isothiazol-5-yl]-carbamic acid phenyl ester

Product 1

HCID 10029921HCID 10029921, compound

Procedure

The title compound was prepared from [4-carbamoyl-3-(2,3,6-trifluoro-4-methyl-benzyloxy)-isothiazol-5-yl]-carbamic acid phenyl ester and 5-amino-1-piperidin-1-yl-pentan-2-ol by the procedure analogous to Example 1. MS (APCl, m/z): 530 [M+H]+.

Sources & evidence

ORD record
ord-b6570a17814e4c778f0f3406c6edfcbd
Source dataset
uspto-grants-2008_07
Patent number
US07405218B2

Reaction notes

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