2-(1-Hydroxycyclohexyl)acetic acid → HCID 178520410, compound

HRID 1023224Notes

Reaction equation

HRID 1023224 reaction equation
Cl.Cl.Cl.[O:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[C:12]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH2:27])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[C:7]=2[O:6][CH2:5]1.[OH:28][C:29]1([CH2:35][C:36](O)=[O:37])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1>>[O:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[C:12]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH:27][C:36](=[O:37])[CH2:35][C:29]5([OH:28])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]5)[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[C:7]=2[O:6][CH2:5]1

Participants

3

Procedure

The title compound, off-white solid (13.4 mg, 40%), MS (ISP) m/z=472.5 [(M+H)+], was prepared in accordance with the general method of example 1 from Trans-4-[2-(4-Benzo[1,3]dioxol-4-yl-piperazin-1-yl)-ethyl]-cyclohexylamine hydrochloride (Intermediate A) (25.8 mg, 0.070 mmol) and 2-(1-hydroxycyclohexyl)acetic acid.

Sources & evidence

ORD record
ord-eddd8fea7b2143adbc4f9976454f2fc7
Source dataset
uspto-grants-2014_05
Patent number
US08722683B2

Reaction notes

Loading…