2-(Oxolan-2-yl)acetic acid → HCID 178520298, compound

HRID 1909363Notes

Reaction equation

HRID 1909363 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]1[CH2:30][CH2:29][CH2:28][CH:27]1[CH2:31][C:32](O)=[O:33]>>[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](=[O:33])[CH2:31][CH:27]5[CH2:28][CH2:29][CH2:30][O:26]5)[CH2:23][CH2:24]4)[CH2:13][CH2:12]3)[C:5]=2[O:4][CH2:3]1

Participants

3

Reactant 2

HCID 2287262-(Oxolan-2-yl)acetic acidHCID 178479251HCID 178479251, compound2×

Product 1

HCID 178520298HCID 178520298, compound

Procedure

The title compound, white solid (9 mg, 25%), MS (ISP) m/z=443.5 [(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) (29.4 mg, 0.080 mmol) and 2-(tetrahydrofuran-2-yl)acetic acid.

Sources & evidence

ORD record
ord-1cb4f0cb2596499ca6139b9151df24a6
Source dataset
uspto-grants-2013_12
Patent number
US08598357B2

Reaction notes

Loading…