HCID 14835022, compound → HCID 15667301, compound

HRID 728474Notes

Reaction equation

HRID 728474 reaction equation
[O:1]1[CH:5]=[CH:4][C:3]([O:6][CH:7]([CH3:32])[CH:8](N)[O:9][C:10](=[O:30])[NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[N:2]1.[Cl:33][CH2:34][CH2:35][CH2:36][S:37]([NH:40]CC(OC)CSCCCCCCCCCCCCCCCC)(=[O:39])=[O:38]>>[Cl:33][CH2:34][CH2:35][CH2:36][S:37]([NH:40][CH2:32][CH:7]([O:6][C:3]1[CH:4]=[CH:5][O:1][N:2]=1)[CH2:8][O:9][C:10](=[O:30])[NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])(=[O:39])=[O:38]

Participants

3

Procedure

2-(3-Isoxazolyloxy)-1-octadecylcarbamoyloxypropylamine IVj2 is allowed to react and worked up by the same procedure as described in (4). m.p. 63.5°-65° C. The summary of the experimental condition and the physical data of the product are listed in Table 7.

Workup

  1. customto react

Sources & evidence

ORD record
ord-6e6587590c04462f8488016f954df11f
Source dataset
uspto-grants-1991_09
Patent number
US05047540

Reaction notes

Loading…