2-(1-Hydroxycyclohexyl)acetic acid → HCID 178520409, compound

HRID 1909378Notes

Reaction equation

HRID 1909378 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.[OH:26][C:27]1([CH2:33][C:34](O)=[O:35])[CH2:32][CH2:31][CH2:30][CH2:29][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:34](=[O:35])[CH2:33][C:27]5([OH:26])[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]5)[CH2:23][CH2:24]4)[CH2:13][CH2:12]3)[C:5]=2[O:4][CH2:3]1

Participants

3

Reactant 2

HCID 2481532-(1-Hydroxycyclohexyl)acetic acidHCID 178479251HCID 178479251, compound2×

Product 1

HCID 178520409HCID 178520409, compound

Procedure

The title compound, light yellow solid (21.3 mg, 64.7%), MS (ISP) m/z=471.5[(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) (25.7 mg, 0.07 mmol) and 2-(1-hydroxycyclohexyl)acetic acid

Sources & evidence

ORD record
ord-4f0fae1cdafd40bca8e63f78b4245cc2
Source dataset
uspto-grants-2013_12
Patent number
US08598357B2

Reaction notes

Loading…